A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3655013



Internal ID18953294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:3907023..3946124hg38UCSC Ensembl
Innerchr7:3946655..3985756hg19UCSC Ensembl
Innerchr7:3913181..3952282hg18UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg3839102
hg1939102
hg1839102
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1020222
Supporting Variants
Samples
Known GenesSDK1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3655013
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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