A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1078059



Internal ID15931245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:1121522..1181464hg38UCSC Ensembl
Innerchr7:1161158..1221100hg19UCSC Ensembl
Innerchr7:1127684..1187626hg18UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3859943
hg1959943
hg1859943
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605736
Supporting Variants
Samples
Known GenesC7orf50, ZFAND2A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1078059
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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