A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1099470



Internal ID15605970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:149421444..149499939hg38UCSC Ensembl
Innerchr7:149118535..149197030hg19UCSC Ensembl
Innerchr7:148749468..148827963hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3878496
hg1978496
hg1878496
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv608978
Supporting Variants
Samples
Known GenesZNF746, ZNF777
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1099470
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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