A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575956



Internal ID16363365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:72268638..72296621hg38UCSC Ensembl
Innerchr17:70264779..70292762hg19UCSC Ensembl
Innerchr17:67776374..67804357hg18UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3827984
hg1927984
hg1827984
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149801
Samples1780854393_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575956
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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