A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13696632



Internal ID21218484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:38631084..38631133hg38UCSC Ensembl
chr17:36787337..36787386hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2797763
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13696632
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.409091


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