A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015639



Internal ID18758173
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:5169879..5215768hg38UCSC Ensembl
Innerchr7:5209510..5255399hg19UCSC Ensembl
Innerchr7:5176036..5221925hg18UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg3845890
hg1945890
hg1845890
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655057
Samples
Known GenesWIPI2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015639
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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