A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572834



Internal ID16360243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:60035366..60114910hg38UCSC Ensembl
Innerchr16:60069270..60148814hg19UCSC Ensembl
Innerchr16:58626771..58706315hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3879545
hg1979545
hg1879545
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149171, nssv1149170
SamplesNINDS_212, HGDP00109
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572834
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