A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2758209



Internal ID17883639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:104614617..104618850hg38UCSC Ensembl
Innerchr9:107376898..107381131hg19UCSC Ensembl
Innerchr9:106416719..106420952hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg384234
hg194234
hg184234
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv969772
Supporting Variants
SamplesHGDP01307
Known GenesOR13C9
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2758209
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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