A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945824



Internal ID18592674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:23243954..23245267hg38UCSC Ensembl
Innerchr1:23570447..23571760hg19UCSC Ensembl
Innerchr1:23443034..23444347hg18UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg381314
hg191314
hg181314
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1765199, nssv1765204, nssv1765202, nssv1765200, nssv1765206, nssv1765205, nssv1765203, nssv1765207, nssv1765198, nssv1765201
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)nsv945824
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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