A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982335



Internal ID18270844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:105758488..105769044hg38UCSC Ensembl
Innerchr9:108520769..108531325hg19UCSC Ensembl
Innerchr9:107560590..107571146hg18UCSC Ensembl
Cytoband9q31.2
Allele length
AssemblyAllele length
hg3810557
hg1910557
hg1810557
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2563285, nssv2563288, nssv2563286, nssv2563287, nssv2563283, nssv2563282, nssv2563284, nssv2563291, nssv2563290, nssv2563289
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)nsv982335
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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