A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv962452



Internal ID18251009
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 Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2763664
SamplesHGDP00456
Known GenesTRIM37
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv962452
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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