A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948175



Internal ID18248335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:103245020..103247057hg38UCSC Ensembl
Innerchr10:105004777..105006814hg19UCSC Ensembl
Innerchr10:104994767..104996804hg18UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg382038
hg192038
hg182038
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1865303, nssv1865310, nssv1865305, nssv1865301, nssv1865306, nssv1865308, nssv1865309, nssv1865302, nssv1865307, nssv1865304
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLOC729020
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv948175
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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