A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945724



Internal ID18592575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:628516..634676hg38UCSC Ensembl
Innerchr1:563896..570056hg19UCSC Ensembl
Innerchr1:553759..559919hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg386161
hg196161
hg186161
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1749675, nssv1749674, nssv1749667, nssv1749676, nssv1749668, nssv1749669, nssv1749670, nssv1749672, nssv1749671, nssv1749673
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesMIR6723
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv945724
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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