A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574432



Internal ID16361841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:15124688..15154919hg38UCSC Ensembl
Innerchr17:15028005..15058236hg19UCSC Ensembl
Innerchr17:14968730..14998961hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3830232
hg1930232
hg1830232
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5462n54
Supporting Variantsnssv1149734, nssv1149733
SamplesHGDP01399, HGDP00812
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574432
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer