A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1141635



Internal ID15648135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:127870731..127873658hg38UCSC Ensembl
Innerchr9:130633010..130635937hg19UCSC Ensembl
Innerchr9:129672831..129675758hg18UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg382928
hg192928
hg182928
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv615379
Supporting Variants
Samples
Known GenesAK1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1141635
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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