A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947980



Internal ID18594826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:49771194..49774822hg38UCSC Ensembl
Innerchr10:50979240..50982868hg19UCSC Ensembl
Innerchr10:50649246..50652874hg18UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg383629
hg193629
hg183629
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1848135, nssv1848143, nssv1848142, nssv1848141, nssv1848138, nssv1848137, nssv1848140, nssv1848139, nssv1848136, nssv1848144
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv947980
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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