A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15186639



Internal ID21325461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:16225124..16225124hg38UCSC Ensembl
chr2:16406392..16406392hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg38392
hg19392
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3936652
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15186639
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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