A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968724



Internal ID18603952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:89449619..89452015hg38UCSC Ensembl
Innerchr9:92064534..92066930hg19UCSC Ensembl
Innerchr9:91254354..91256750hg18UCSC Ensembl
Cytoband9q22.2
Allele length
AssemblyAllele length
hg382397
hg192397
hg182397
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2559035, nssv2559037, nssv2559043, nssv2559036, nssv2559034, nssv2559039, nssv2559038, nssv2559042, nssv2559040, nssv2559041
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesSEMA4D
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv968724
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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