A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1148345



Internal ID15654845
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 StatusS
Merged Variantsnsv615993
Supporting Variants
Samples
Known GenesLCNL1, PTGDS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1148345
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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