A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972664



Internal ID18607880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:34917468..34922945hg38UCSC Ensembl
Innerchr9:34917465..34922942hg19UCSC Ensembl
Innerchr9:34907465..34912942hg18UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg385478
hg195478
hg185478
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2528474, nssv2528482, nssv2528478, nssv2528476, nssv2528477, nssv2528480, nssv2528475, nssv2528479, nssv2528483, nssv2528481
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972664
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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