A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615611



Internal ID16056334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:133101292..133167883hg38UCSC Ensembl
Innerchr9:135976679..136043270hg19UCSC Ensembl
Innerchr9:134966500..135033091hg18UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg3866592
hg1966592
hg1866592
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12928n54
Supporting Variantsnssv1145400
Samples
Known GenesGBGT1, RALGDS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615611
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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