A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574107



Internal ID16361516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:948888..949686hg38UCSC Ensembl
Innerchr17:852128..852926hg19UCSC Ensembl
Innerchr17:798878..799676hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg38799
hg19799
hg18799
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5395n54
Supporting Variantsnssv865892, nssv865901, nssv865876, nssv865896, nssv865899, nssv865887, nssv865880, nssv865905, nssv865872, nssv865897, nssv865889, nssv865906, nssv865895, nssv865898, nssv865886, nssv865902, nssv865875, nssv865903, nssv865894, nssv865888, nssv865874, nssv865900, nssv865884, nssv865890, nssv865883, nssv865878, nssv865873, nssv865907, nssv865877, nssv865882, nssv865904, nssv865908, nssv865885, nssv865881, nssv865891, nssv865893, nssv865879
Samples
Known GenesNXN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574107
Frequency
Sample Size17421
Observed Gain29
Observed Loss8
Observed Complex0
Frequencyn/a


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