A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13707449



Internal ID21229241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:84080546..84080871hg38UCSC Ensembl
chr7:83709862..83710187hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2817103
Supporting Variants
Samples
Known GenesSEMA3A
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13707449
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.921875


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