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dbVar

Database of genomic structural variation

nsv3068935

Organism: Homo sapiens

Study:nstd90 (dbSNP curated variants)
Variant Type:copy number variation
Method Type:Curated
Submitted on:GRCh37 (hg19)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:876

Data Source:HUMANGENOME_JCVI

Links to Other Resources

Source: NCBI

Genome View
Variant Region Details and Evidence
Validation Information
Clinical Assertions
Genotype Information

Genome View

Select assembly:

Overlapping variant regions from other studies: 755 SVs from 58 studies. See in: genome view

Remapped(Score: Perfect):1,526,402-1,527,277

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Start	Stop
nsv3068935	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000002.12	Chr2	1,526,402	1,527,277
nsv3068935	Remapped	Perfect	GRCh38.p12	ALT_REF_LOCI_1	Second Pass	NT_187529.1	Chr2\|NT_18 7529.1	208,773	209,648
nsv3068935	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000002.11	Chr2	1,530,174	1,531,049

Variant Call Information

Variant Call ID	Type	Sample ID	Method	Analysis
nssv14039745	deletion	1104685022645	Curated	Curated

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Start	Stop
nssv14039745	Remapped	Perfect	NT_187529.1:g.2087 73_209648del876	GRCh38.p12	Second Pass	NT_187529.1	Chr2\|NT_18 7529.1	208,773	209,648
nssv14039745	Remapped	Perfect	NC_000002.12:g.152 6402_1527277del876	GRCh38.p12	First Pass	NC_000002.12	Chr2	1,526,402	1,527,277
nssv14039745	Submitted genomic		NC_000002.11:g.153 0174_1531049del876	GRCh37 (hg19)		NC_000002.11	Chr2	1,530,174	1,531,049

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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