A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947863



Internal ID18594710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:38575705..38605739hg38UCSC Ensembl
Innerchr10:38868836..38898870hg19UCSC Ensembl
Innerchr10:38908632..38938876hg18UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg3830035
hg1930035
hg1830245
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1840887, nssv2607287, nssv1840895, nssv2607284, nssv2607279, nssv2607311, nssv2607281, nssv2607278, nssv2607286, nssv1840888, nssv2607282, nssv2607313, nssv2607312, nssv2607320, nssv2607317, nssv1840894, nssv1840891, nssv1840892, nssv2607318, nssv2607280, nssv2607283, nssv2607316, nssv1840889, nssv2607314, nssv1840896, nssv1840890, nssv2607315, nssv1840893, nssv2607319, nssv2607285
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
lineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv947863
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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