A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024704



Internal ID19113921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:3696622..3792227hg38UCSC Ensembl
Innerchr7:3736254..3831859hg19UCSC Ensembl
Innerchr7:3702780..3798385hg18UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg3895606
hg1995606
hg1895606
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6228n100
Supporting Variantsnssv3655010
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)nsv1024704
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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