A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945826



Internal ID18592676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:23942157..23949216hg38UCSC Ensembl
Innerchr1:24268647..24275706hg19UCSC Ensembl
Innerchr1:24141234..24148293hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg387060
hg197060
hg187060
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1764968, nssv1764973, nssv1764967, nssv1764975, nssv1764971, nssv1764970, nssv1764969, nssv1764972, nssv1764974, nssv1764966
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)nsv945826
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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