A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv13707407



Internal ID21229200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:38631161..38631238hg38UCSC Ensembl
chr17:36787414..36787491hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2797580
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nssv13707407
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.333333


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