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dbVar

Database of genomic structural variation

nsv4410067

Organism: Homo sapiens

Study:nstd174 (DGV Gold Standard)
Variant Type:copy number variation
Method Type:Multiple
Submitted on:GRCh37 (hg19)

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:102,300

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: 888 SVs from 75 studies. See in: genome view

Remapped(Score: Perfect):143,243,031-143,345,330

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop
nsv4410067	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000008.11	Chr8	143,243,031	143,243,031	143,345,330	143,345,330
nsv4410067	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000008.10	Chr8	144,325,201	144,325,201	144,427,500	144,427,500

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv15743441	copy number loss	Multiple	Multiple

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Outer Start	Inner Start	Inner Stop	Outer Stop
nssv15743441	Remapped	Perfect	NC_000008.11:g.(14 3243031_143243031) _(143345330_143345 330)del	GRCh38.p12	First Pass	NC_000008.11	Chr8	143,243,031	143,243,031	143,345,330	143,345,330
nssv15743441	Submitted genomic		NC_000008.10:g.(14 4325201_144325201) _(144427500_144427 500)del	GRCh37 (hg19)		NC_000008.10	Chr8	144,325,201	144,325,201	144,427,500	144,427,500

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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