A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575688



Internal ID16363097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:55566985..55656663hg38UCSC Ensembl
Innerchr17:53644346..53734024hg19UCSC Ensembl
Innerchr17:50999345..51089023hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3889679
hg1989679
hg1889679
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv874121
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575688
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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