A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15176460



Internal ID21315256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:100922995..100923315hg38UCSC Ensembl
chr1:101388551..101388871hg19UCSC Ensembl
Cytoband1p21.2
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3933521
Supporting Variants
SamplesHG002
Known GenesSLC30A7
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15176460
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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