A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574093



Internal ID16361502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:820999..821306hg38UCSC Ensembl
Innerchr17:724239..724546hg19UCSC Ensembl
Innerchr17:670989..671296hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38308
hg19308
hg18308
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5393n54
Supporting Variantsnssv865139, nssv865125, nssv865124, nssv865115, nssv865118, nssv865141, nssv865128, nssv865144, nssv865138, nssv865133, nssv865137, nssv865120, nssv865130, nssv865136, nssv865127, nssv865119, nssv865134, nssv865131, nssv865123, nssv865121, nssv865117, nssv865142, nssv865122, nssv865114, nssv865143, nssv865132, nssv865140, nssv865135, nssv865126, nssv865129, nssv865116
Samples
Known GenesNXN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574093
Frequency
Sample Size17421
Observed Gain0
Observed Loss31
Observed Complex0
Frequencyn/a


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