A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3642992



Internal ID18941273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:13053579..13090444hg38UCSC Ensembl
Innerchr7:13093204..13130069hg19UCSC Ensembl
Innerchr7:13059729..13096594hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3836866
hg1936866
hg1836866
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1027572
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3642992
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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