A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1089387



Internal ID15942573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:87687838..87696630hg38UCSC Ensembl
Innerchr7:87317154..87325946hg19UCSC Ensembl
Innerchr7:87155090..87163882hg18UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg388793
hg198793
hg188793
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607728
Supporting Variants
Samples
Known GenesABCB1, RUNDC3B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1089387
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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