A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968732



Internal ID18603960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:94281229..94288510hg38UCSC Ensembl
Innerchr9:97043511..97050792hg19UCSC Ensembl
Innerchr9:96083332..96090613hg18UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg387282
hg197282
hg187282
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2559807, nssv2559806, nssv2559809, nssv2559811, nssv2559808, nssv2559805, nssv2559810, nssv2559812, nssv2559813, nssv2559814
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesZNF169
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv968732
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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