A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972798



Internal ID18608014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:103999799..104005070hg38UCSC Ensembl
Innerchr9:106762080..106767351hg19UCSC Ensembl
Innerchr9:105801901..105807172hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg385272
hg195272
hg185272
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2564326, nssv2564328, nssv2564323, nssv2564330, nssv2564327, nssv2564324, nssv2564329, nssv2564331, nssv2564821, nssv2564325
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesMIR6130
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972798
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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