A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17030275



Internal ID87897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13472950..13473573hg38UCSC Ensembl
chr10:13514950..13515573hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38624
hg19624
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5474452
Supporting Variants
Samples
Known GenesBEND7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17030275
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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