A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1156875



Internal ID15533015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:125055955..125120574hg38UCSC Ensembl
Innerchr8:126068197..126132816hg19UCSC Ensembl
Innerchr8:126137379..126201998hg18UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg3864620
hg1964620
hg1864620
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv612148
Supporting Variants
SamplesHGDP01418
Known GenesKIAA0196, NSMCE2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1156875
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