A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947730



Internal ID18594577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:5775725..5785275hg38UCSC Ensembl
Innerchr10:5817688..5827238hg19UCSC Ensembl
Innerchr10:5857694..5867244hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg389551
hg199551
hg189551
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1831476, nssv1831477, nssv1831479, nssv1831472, nssv1831475, nssv1831473, nssv1831474, nssv1831480, nssv1831478, nssv1831481
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesGDI2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv947730
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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