A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1083229



Internal ID15589729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:44107807..44114893hg38UCSC Ensembl
Innerchr7:44147406..44154492hg19UCSC Ensembl
Innerchr7:44113931..44121017hg18UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg387087
hg197087
hg187087
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv606750
Supporting Variants
Samples
Known GenesAEBP1, MIR4649, POLD2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1083229
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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