A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982455



Internal ID18617650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:62389743..62405782hg38UCSC Ensembl
Innerchr9:46701044..46717083hg19UCSC Ensembl
Innerchr9:46541040..46557079hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3816040
hg1916040
hg1816040
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2737616, nssv2737614, nssv2737611, nssv2737615, nssv2737618, nssv2737613, nssv2737620, nssv2737617, nssv2737612, nssv2737619
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesKGFLP1, LOC643648
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982455
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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