A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615993



Internal ID16056716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:136975638..136983246hg38UCSC Ensembl
Innerchr9:139870090..139877698hg19UCSC Ensembl
Innerchr9:138989911..138997519hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg387609
hg197609
hg187609
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1148345
Samples
Known GenesLCNL1, PTGDS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615993
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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