A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1083680



Internal ID15936866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:47050045..47052691hg38UCSC Ensembl
Innerchr7:47089643..47092289hg19UCSC Ensembl
Innerchr7:47056168..47058814hg18UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg382647
hg192647
hg182647
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv606856
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1083680
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