A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1078805



Internal ID15931991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:4780950..4801718hg38UCSC Ensembl
Innerchr7:4820581..4841349hg19UCSC Ensembl
Innerchr7:4787107..4807875hg18UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg3820769
hg1920769
hg1820769
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605977
Supporting Variants
Samples
Known GenesAP5Z1, MIR4656, RADIL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1078805
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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