A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945739



Internal ID18592590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:865934..891159hg38UCSC Ensembl
Innerchr1:801314..826539hg19UCSC Ensembl
Innerchr1:791177..816402hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3825226
hg1925226
hg1825226
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1753187, nssv1752259, nssv1753185, nssv1753192, nssv1753191, nssv1753186, nssv1753184, nssv1753188, nssv1753189, nssv1753190
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesFAM41C
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv945739
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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