A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972349



Internal ID18607565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:42726446..42740370hg38UCSC Ensembl
Innerchr9:44230749..44244724hg19UCSC Ensembl
Innerchr9:44170745..44184720hg18UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3813925
hg1913976
hg1813976
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2539912, nssv2539906, nssv2539915, nssv2539907, nssv2539910, nssv2539908, nssv2539909, nssv2539914, nssv2539913, nssv2539911
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)nsv972349
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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