A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv946032



Internal ID18592882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:83270193..83361303hg38UCSC Ensembl
Innerchr1:83735876..83826986hg19UCSC Ensembl
Innerchr1:83508464..83599574hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3891111
hg1991111
hg1891111
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1773541, nssv1773535, nssv1773538, nssv1773537, nssv1773540, nssv1773539, nssv1773536, nssv1773543, nssv1773534, nssv1773542
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)nsv946032
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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