A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945697



Internal ID18245862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:10001..19818hg38UCSC Ensembl
Innerchr1:10001..19818hg19UCSC Ensembl
Innerchr1:1..9681hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg389818
hg199818
hg189681
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1n82
Supporting Variantsnssv1751754, nssv1751732, nssv1751776, nssv1751810, nssv1751799, nssv1751765, nssv1750595, nssv1751743, nssv1751788, nssv1750706
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesDDX11L1, LOC100288778, MIR6859-1, MIR6859-2, WASH7P
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv945697
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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