A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608215



Internal ID16395624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:111543554..111893464hg38UCSC Ensembl
Innerchr7:111183610..111533520hg19UCSC Ensembl
Innerchr7:110970846..111320756hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38349911
hg19349911
hg18349911
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1092741
Samples
Known GenesDOCK4, DOCK4-AS1, IMMP2L
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608215
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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