A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17628237



Internal ID21820284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:87983173..87983173hg38UCSC Ensembl
chr16:88016779..88016779hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg383168
hg193168
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6088576
Supporting Variants
Samples
Known GenesBANP
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17628237
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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