A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982305



Internal ID18617500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:72470465..72471716hg38UCSC Ensembl
Innerchr9:75085381..75086632hg19UCSC Ensembl
Innerchr9:74275201..74276452hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg381252
hg191252
hg181252
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2551836, nssv2551831, nssv2551839, nssv2551840, nssv2551838, nssv2551832, nssv2551833, nssv2551834, nssv2551835, nssv2551837
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)nsv982305
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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