A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605893



Internal ID16393302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:3328565..3465599hg38UCSC Ensembl
Innerchr7:3368197..3505231hg19UCSC Ensembl
Innerchr7:3334723..3471757hg18UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg38137035
hg19137035
hg18137035
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1078499, nssv1078500
Samples
Known GenesSDK1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605893
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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