A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1093598



Internal ID15946784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:123328044..123391378hg38UCSC Ensembl
Innerchr7:122968098..123031432hg19UCSC Ensembl
Innerchr7:122755334..122818668hg18UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg3863335
hg1963335
hg1863335
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv608337
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1093598
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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