A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17600706



Internal ID21792753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:41074140..41074196hg38UCSC Ensembl
chr13:41648276..41648332hg19UCSC Ensembl
Cytoband13q14.11
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6024875
Supporting Variants
Samples
Known GenesWBP4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17600706
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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