A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947853



Internal ID18248014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:38013010..38017473hg38UCSC Ensembl
Innerchr10:38301938..38306401hg19UCSC Ensembl
Innerchr10:38341944..38346407hg18UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg384464
hg194464
hg184464
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1840399, nssv1840403, nssv1840394, nssv1840400, nssv1840398, nssv1840396, nssv1840397, nssv1840401, nssv1840395, nssv1840402
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesZNF33A
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv947853
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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