A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1094501



Internal ID15601001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:128794846..128876416hg38UCSC Ensembl
Innerchr7:128434900..128516470hg19UCSC Ensembl
Innerchr7:128222136..128303706hg18UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg3881571
hg1981571
hg1881571
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv608402
Supporting Variants
Samples
Known GenesATP6V1F, CCDC136, FLNC, LOC100130705
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1094501
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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