A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574105



Internal ID16361514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:948888..949579hg38UCSC Ensembl
Innerchr17:852128..852819hg19UCSC Ensembl
Innerchr17:798878..799569hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38692
hg19692
hg18692
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5395n54
Supporting Variantsnssv865856, nssv865864, nssv865865, nssv865869, nssv865863, nssv865860, nssv865855, nssv865866, nssv865858, nssv865867, nssv865857, nssv865862, nssv865868, nssv865861, nssv865859
Samples
Known GenesNXN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574105
Frequency
Sample Size17421
Observed Gain8
Observed Loss7
Observed Complex0
Frequencyn/a


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