A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575656



Internal ID16363065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:54491945..54509547hg38UCSC Ensembl
Innerchr17:52569306..52586908hg19UCSC Ensembl
Innerchr17:49924305..49941907hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3817603
hg1917603
hg1817603
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150566
Samples1780862042_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575656
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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