A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv615889



Internal ID16403298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:135579537..135588323hg38UCSC Ensembl
Innerchr9:138471383..138480169hg19UCSC Ensembl
Innerchr9:137611204..137619990hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg388787
hg198787
hg188787
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv12983n54
Supporting Variantsnssv1147145
Samples
Known GenesLOC100130954
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv615889
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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