A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947744



Internal ID18247905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:14723244..14724898hg38UCSC Ensembl
Innerchr10:14765243..14766897hg19UCSC Ensembl
Innerchr10:14805249..14806903hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg381655
hg191655
hg181655
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1830943, nssv1830945, nssv1830950, nssv1830941, nssv1830944, nssv1830947, nssv1830942, nssv1830948, nssv1830946, nssv1830949
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesFAM107B
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv947744
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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