A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972429



Internal ID18607645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:96780038..96786124hg38UCSC Ensembl
Innerchr9:99542320..99548406hg19UCSC Ensembl
Innerchr9:98582141..98588227hg18UCSC Ensembl
Cytoband9q22.33
Allele length
AssemblyAllele length
hg386087
hg196087
hg186087
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2561885, nssv2561888, nssv2561880, nssv2561883, nssv2561882, nssv2561889, nssv2561887, nssv2561886, nssv2561881, nssv2561884
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)nsv972429
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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