A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2763664



Internal ID17389221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:59032160..59048478hg38UCSC Ensembl
Innerchr17:57109521..57125839hg19UCSC Ensembl
Innerchr17:54464303..54480621hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3816319
hg1916319
hg1816319
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv962452
Supporting Variants
SamplesHGDP00456
Known GenesTRIM37
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2763664
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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