A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982268



Internal ID18617463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:62470876..62478388hg38UCSC Ensembl
Innerchr9:46782177..46789689hg19UCSC Ensembl
Innerchr9:46622173..46629685hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg387513
hg197513
hg187513
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv90n82
Supporting Variantsnssv2737637, nssv2737640, nssv2737642, nssv2737635, nssv2737639, nssv2737634, nssv2737641, nssv2737643, nssv2737636, nssv2737638
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982268
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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