A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948034



Internal ID18594880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:63427259..63428060hg38UCSC Ensembl
Innerchr10:65187019..65187820hg19UCSC Ensembl
Innerchr10:64857025..64857826hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38802
hg19802
hg18802
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1853982, nssv1853976, nssv1853978, nssv1853977, nssv1853975, nssv1853979, nssv1853973, nssv1853981, nssv1853980, nssv1853974
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesJMJD1C
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv948034
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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