A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947811



Internal ID18594658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:30611901..30612901hg38UCSC Ensembl
Innerchr10:30900830..30901830hg19UCSC Ensembl
Innerchr10:30940836..30941836hg18UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg381001
hg191001
hg181001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1837472, nssv1837469, nssv1837473, nssv1837474, nssv1837471, nssv1837468, nssv1837470, nssv1837467, nssv1837476, nssv1837475
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLYZL2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv947811
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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