A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945817



Internal ID18592667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:22078110..22078778hg38UCSC Ensembl
Innerchr1:22404603..22405271hg19UCSC Ensembl
Innerchr1:22277190..22277858hg18UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg38669
hg19669
hg18669
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1763838, nssv1763839, nssv1763843, nssv1763844, nssv1763841, nssv1763835, nssv1763842, nssv1763837, nssv1763840, nssv1763836
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCDC42
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv945817
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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