A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982323



Internal ID18617518
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:94363023..94375439hg38UCSC Ensembl
Innerchr9:97125305..97137721hg19UCSC Ensembl
Innerchr9:96165126..96177542hg18UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3812417
hg1912417
hg1812417
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2559127, nssv2559123, nssv2559129, nssv2559125, nssv2559128, nssv2559122, nssv2559126, nssv2559121, nssv2559124, nssv2559120
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesHIATL1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982323
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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