A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1086694



Internal ID15939880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:74102784..74169896hg38UCSC Ensembl
Innerchr7:73517114..73584226hg19UCSC Ensembl
Innerchr7:73155050..73222162hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3867113
hg1967113
hg1867113
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607479
Supporting Variants
Samples
Known GenesLIMK1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1086694
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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