A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615368



Internal ID16056091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:127504287..127547894hg38UCSC Ensembl
Innerchr9:130266566..130310173hg19UCSC Ensembl
Innerchr9:129306387..129349994hg18UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg3843608
hg1943608
hg1843608
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176496
SamplesHGDP00776
Known GenesFAM129B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615368
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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