A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1094787



Internal ID15947973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:137061860..137154643hg38UCSC Ensembl
Innerchr7:136746607..136839390hg19UCSC Ensembl
Innerchr7:136397147..136489930hg18UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3892784
hg1992784
hg1892784
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv608462
Supporting Variants
Samples
Known GenesLOC349160
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1094787
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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