A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574634



Internal ID16362043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:26936561..26958643hg38UCSC Ensembl
Innerchr17:25263587..25285669hg19UCSC Ensembl
Innerchr17:22287714..22309796hg18UCSC Ensembl
Cytoband17q11.1
Allele length
AssemblyAllele length
hg3822083
hg1922083
hg1822083
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5510n54
Supporting Variantsnssv868975
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574634
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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