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dbVar

Database of genomic structural variation

nsv6290102

Organism: Homo sapiens

Study:nstd218 (Wijesiriwardhana et al. 2021)
Variant Type:copy number variation
Method Type:Oligo aCGH
Submitted on:GRCh37

Variant Calls:1
Validation:Not tested
Clinical Assertions: No
Region Size:47,158

Publication(s):Wijesiriwardhana et al. 2021

Links to Other Resources

Overlapping Genes

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: 166 SVs from 29 studies. See in: genome view

Remapped(Score: Perfect):105,376,205-105,423,362

Variant Region Placement Information

Variant Region ID	Placement Type	Score	Assembly	Assembly Unit	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nsv6290102	Remapped	Perfect	GRCh38.p12	Primary Assembly	First Pass	NC_000006.12	Chr6	105,376,205	105,423,362
nsv6290102	Submitted genomic		GRCh37 (hg19)	Primary Assembly		NC_000006.11	Chr6	105,824,080	105,871,237

Variant Call Information

Variant Call ID	Type	Method	Analysis
nssv17955715	copy number gain	Oligo aCGH	Probe signal intensity

Variant Call Placement Information

Variant Call ID	Placement Type	Score	HGVS	Assembly	Reciprocity	Sequence ID	Chr	Inner Start	Inner Stop
nssv17955715	Remapped	Perfect	NC_000006.12:g.(?_ 105376205)_(105423 362_?)dup	GRCh38.p12	First Pass	NC_000006.12	Chr6	105,376,205	105,423,362
nssv17955715	Submitted genomic		NC_000006.11:g.(?_ 105824080)_(105871 237_?)dup	GRCh37 (hg19)		NC_000006.11	Chr6	105,824,080	105,871,237

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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