A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945935



Internal ID18592785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:50323777..50328494hg38UCSC Ensembl
Innerchr1:50789449..50794166hg19UCSC Ensembl
Innerchr1:50562036..50566753hg18UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg384718
hg194718
hg184718
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1764535, nssv1764537, nssv1764532, nssv1764530, nssv1764538, nssv1764531, nssv1764533, nssv1764529, nssv1764534, nssv1764536
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)nsv945935
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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