A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv969772



Internal ID18604999
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 Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2759906, nssv2759895, nssv2762721, nssv2764907, nssv2765066, nssv2758683, nssv2760695, nssv2758209, nssv2766710
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP00456, HGDP00927
Known GenesOR13C9
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv969772
Frequency
Sample Size10
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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