A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1155228



Internal ID15533120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:128818595..128928906hg38UCSC Ensembl
Innerchr7:128458649..128568960hg19UCSC Ensembl
Innerchr7:128245885..128356196hg18UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg38110312
hg19110312
hg18110312
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv608404
Supporting Variants
SamplesNINDS_111
Known GenesATP6V1F, CCDC136, FLNC, KCP, LOC100130705
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1155228
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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