A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1089388



Internal ID15942574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:87697613..87723256hg38UCSC Ensembl
Innerchr7:87326929..87352572hg19UCSC Ensembl
Innerchr7:87164865..87190508hg18UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg3825644
hg1925644
hg1825644
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607729
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)nssv1089388
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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