A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945840



Internal ID18246004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:26426339..26429437hg38UCSC Ensembl
Innerchr1:26752830..26755928hg19UCSC Ensembl
Innerchr1:26625417..26628515hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg383099
hg193099
hg183099
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1765440, nssv1765438, nssv1765436, nssv1765437, nssv1765439, nssv1765442, nssv1765441, nssv1765444, nssv1765445, nssv1765443
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLIN28A
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv945840
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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