A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13706709



Internal ID21228437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:96378192..96378192hg38UCSC Ensembl
chr7:96007504..96007504hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2816840
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13706709
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequency1


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