A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615640



Internal ID16403049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:133650175..133663599hg38UCSC Ensembl
Innerchr9:136515297..136528721hg19UCSC Ensembl
Innerchr9:135505118..135518542hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3813425
hg1913425
hg1813425
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176521
SamplesHGDP00961
Known GenesDBH, DBH-AS1, SARDH
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615640
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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