A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13705404



Internal ID21227210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:76414814..76414814hg38UCSC Ensembl
chr7:76044131..76044131hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38683
hg19683
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2817090
Supporting Variants
Samples
Known GenesZP3
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13705404
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency1


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