A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17038951



Internal ID93722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:126058612..126439947hg38UCSC Ensembl
chr10:127747181..128128516hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg38381336
hg19381336
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5504265
Supporting Variants
Samples
Known GenesADAM12, C10orf90, LINC00601
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17038951
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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