A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945920



Internal ID18592770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:45607480..45608212hg38UCSC Ensembl
Innerchr1:46073152..46073884hg19UCSC Ensembl
Innerchr1:45845739..45846471hg18UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg38733
hg19733
hg18733
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1762230, nssv1762233, nssv1762235, nssv1762237, nssv1762236, nssv1762239, nssv1762234, nssv1762231, nssv1762238, nssv1762232
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesNASP
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv945920
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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