A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945757



Internal ID18592608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:8057016..8063696hg38UCSC Ensembl
Innerchr1:8117076..8123756hg19UCSC Ensembl
Innerchr1:8039663..8046343hg18UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg386681
hg196681
hg186681
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1750969, nssv1750960, nssv1750964, nssv1750966, nssv1750961, nssv1750963, nssv1750967, nssv1750965, nssv1750968, nssv1750962
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)nsv945757
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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