A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13698148



Internal ID21219998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:81132104..81132104hg38UCSC Ensembl
chr7:80761420..80761420hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2817094
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13698148
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.59375


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