A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1155281



Internal ID15877781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:10126999..10165150hg38UCSC Ensembl
Innerchr7:10166626..10204777hg19UCSC Ensembl
Innerchr7:10133151..10171302hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3838152
hg1938152
hg1838152
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv606185
Supporting Variants
SamplesHGDP01045
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1155281
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