A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615971



Internal ID16056694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:136583078..136670216hg38UCSC Ensembl
Innerchr9:139477530..139564668hg19UCSC Ensembl
Innerchr9:138597351..138684489hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3887139
hg1987139
hg1887139
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176158
SamplesHGDP00445
Known GenesEGFL7
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615971
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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