A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615803



Internal ID16403212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:134271872..134323982hg38UCSC Ensembl
Innerchr9:137163718..137215828hg19UCSC Ensembl
Innerchr9:136303539..136355649hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3852111
hg1952111
hg1852111
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176375
SamplesHGDP00785
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615803
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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