A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1096530



Internal ID15603030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143372217..143425364hg38UCSC Ensembl
Innerchr7:143069310..143122457hg19UCSC Ensembl
Innerchr7:142779432..142832579hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3853148
hg1953148
hg1853148
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv608681
Supporting Variants
Samples
Known GenesEPHA1, EPHA1-AS1, MIR6892, ZYX
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1096530
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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