A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982630



Internal ID18271139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:6672217..6796787hg38UCSC Ensembl
Innerchr9:6672217..6796787hg19UCSC Ensembl
Innerchr9:6662217..6786787hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38124571
hg19124571
hg18124571
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2764425
SamplesHGDP00998
Known GenesKDM4C
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982630
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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