A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1094503



Internal ID15601003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:128832927..128920707hg38UCSC Ensembl
Innerchr7:128472981..128560761hg19UCSC Ensembl
Innerchr7:128260217..128347997hg18UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg3887781
hg1987781
hg1887781
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv608405
Supporting Variants
Samples
Known GenesATP6V1F, FLNC, KCP, LOC100130705
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1094503
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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