A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574992



Internal ID16015715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:39662308..39666058hg38UCSC Ensembl
Innerchr17:37818561..37822311hg19UCSC Ensembl
Innerchr17:35072087..35075837hg18UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg383751
hg193751
hg183751
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv870533
Samples
Known GenesSTARD3, TCAP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574992
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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