A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6145668



Internal ID344873
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:31510415..31511625hg38UCSC Ensembl
chr15:31802618..31803828hg19UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg381211
hg191211
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17701784
Samples
Known GenesOTUD7A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6145668
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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