A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605918



Internal ID16393327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:3608851..3615507hg38UCSC Ensembl
Innerchr7:3648483..3655139hg19UCSC Ensembl
Innerchr7:3615009..3621665hg18UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg386657
hg196657
hg186657
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11154n54
Supporting Variantsnssv1078547
Samples
Known GenesSDK1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605918
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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