A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945520



Internal ID18592371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:481637..485248hg38UCSC Ensembl
Innerchr1:334089..337700hg19UCSC Ensembl
Innerchr1:323952..327563hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg383612
hg193612
hg183612
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2569331, nssv2569327, nssv2569332, nssv2569334, nssv2569328, nssv2569330, nssv2569329, nssv2569333, nssv2569336, nssv2569335
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv945520
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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