A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947747



Internal ID18594594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:15093311..15094693hg38UCSC Ensembl
Innerchr10:15135310..15136692hg19UCSC Ensembl
Innerchr10:15175316..15176698hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg381383
hg191383
hg181383
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1832102, nssv1832101, nssv1832097, nssv1832104, nssv1832099, nssv1832100, nssv1832098, nssv1832096, nssv1832105, nssv1832103
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)nsv947747
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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