A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17604919



Internal ID21796966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2321328..2321328hg38UCSC Ensembl
chr16:2371329..2371329hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6097664
Supporting Variants
Samples
Known GenesABCA3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17604919
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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