A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1155282



Internal ID15877836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:10126999..10180922hg38UCSC Ensembl
Innerchr7:10166626..10220549hg19UCSC Ensembl
Innerchr7:10133151..10187074hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3853924
hg1953924
hg1853924
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv606186
Supporting Variants
SamplesHGDP01052
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1155282
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