A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1094507



Internal ID15601007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:128843173..128911686hg38UCSC Ensembl
Innerchr7:128483227..128551740hg19UCSC Ensembl
Innerchr7:128270463..128338976hg18UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg3868514
hg1968514
hg1868514
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv608409
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)nssv1094507
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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