A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv968742



Internal ID18257284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:105709167..105710527hg38UCSC Ensembl
Innerchr9:108471448..108472808hg19UCSC Ensembl
Innerchr9:107511269..107512629hg18UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg381361
hg191361
hg181361
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2563191, nssv2563188, nssv2563187, nssv2563193, nssv2563186, nssv2563190, nssv2563192, nssv2563194, nssv2563189, nssv2563185
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesTMEM38B
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv968742
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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