A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945906



Internal ID18592756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:42696401..42697030hg38UCSC Ensembl
Innerchr1:43162072..43162701hg19UCSC Ensembl
Innerchr1:42934659..42935288hg18UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg38630
hg19630
hg18630
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1762410, nssv1762408, nssv1762415, nssv1762416, nssv1762409, nssv1762414, nssv1762412, nssv1762413, nssv1762407, nssv1762411
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesYBX1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv945906
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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