A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17029535



Internal ID87382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4881150..4881226hg38UCSC Ensembl
chr10:4923342..4923418hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5481782
Supporting Variants
Samples
Known GenesAKR1C6P
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17029535
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000781


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