A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv609738



Internal ID16397147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:3534678..3566326hg38UCSC Ensembl
Innerchr8:3392200..3423848hg19UCSC Ensembl
Innerchr8:3379608..3411256hg18UCSC Ensembl
Cytoband8p23.2
Allele length
AssemblyAllele length
hg3831649
hg1931649
hg1831649
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1156111
SamplesNINDS_160
Known GenesCSMD1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv609738
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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