A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13685224



Internal ID21207080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:203839994..203839994hg38UCSC Ensembl
chr1:203809122..203809122hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38734
hg19734
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2801263
Supporting Variants
Samples
Known GenesZC3H11A
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13685224
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.140625


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