A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1099474



Internal ID15605974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:149753495..149787971hg38UCSC Ensembl
Innerchr7:149450584..149485059hg19UCSC Ensembl
Innerchr7:149081517..149115992hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3834477
hg1934476
hg1834476
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv608983
Supporting Variants
Samples
Known GenesSSPO, ZNF467
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1099474
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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