A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17599136



Internal ID21791181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:34979916..34979916hg38UCSC Ensembl
chr15:35272117..35272117hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6083647
Supporting Variants
Samples
Known GenesZNF770
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17599136
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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