A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972400



Internal ID18607616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:72740112..72741635hg38UCSC Ensembl
Innerchr9:75355028..75356551hg19UCSC Ensembl
Innerchr9:74544848..74546371hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg381524
hg191524
hg181524
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2552837, nssv2552838, nssv2552843, nssv2552836, nssv2552835, nssv2552839, nssv2552841, nssv2552834, nssv2552842, nssv2552840
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesTMC1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972400
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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