A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17626018



Internal ID21818065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:78111931..78111931hg38UCSC Ensembl
chr17:76108012..76108012hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3898
hg1998
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6097965
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17626018
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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