A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575801



Internal ID16363210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:58630658..58631756hg38UCSC Ensembl
Innerchr17:56708019..56709117hg19UCSC Ensembl
Innerchr17:54063018..54064116hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg381099
hg191099
hg181099
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149778
SamplesHGDP01028
Known GenesTEX14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575801
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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