A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1078619



Internal ID15585119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:3673562..3759948hg38UCSC Ensembl
Innerchr7:3713194..3799580hg19UCSC Ensembl
Innerchr7:3679720..3766106hg18UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg3886387
hg1986387
hg1886387
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605935
Supporting Variants
Samples
Known GenesSDK1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1078619
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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