A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945726



Internal ID18592577
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:634676..682530hg38UCSC Ensembl
Innerchr1:570056..617910hg19UCSC Ensembl
Innerchr1:559919..607773hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3847855
hg1947855
hg1847855
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1749773, nssv1749769, nssv1749767, nssv1749764, nssv1749770, nssv1749765, nssv1749766, nssv1749771, nssv1749768, nssv1749772
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv945726
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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