A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982324



Internal ID18617519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:94376780..94437874hg38UCSC Ensembl
Innerchr9:97139062..97200156hg19UCSC Ensembl
Innerchr9:96178883..96239977hg18UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3861095
hg1961095
hg1861095
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2559132, nssv2559140, nssv2559133, nssv2559137, nssv2559138, nssv2559131, nssv2559139, nssv2559134, nssv2559136, nssv2559135
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)nsv982324
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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