A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17609794



Internal ID21801841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:112572438..112572619hg38UCSC Ensembl
chr12:113010242..113010423hg19UCSC Ensembl
Cytoband12q24.13
Allele length
AssemblyAllele length
hg38182
hg19182
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6020587
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17609794
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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