A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13698455



Internal ID21220304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:128107556..128107556hg38UCSC Ensembl
chr7:127747608..127747608hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg38270
hg19270
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2814237
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13698455
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.142857


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