A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948145



Internal ID18248305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:94774536..94775509hg38UCSC Ensembl
Innerchr10:96534293..96535266hg19UCSC Ensembl
Innerchr10:96524283..96525256hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg38974
hg19974
hg18974
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1862537, nssv1862530, nssv1862538, nssv1862536, nssv1862532, nssv1862534, nssv1862531, nssv1862533, nssv1862539, nssv1862535
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCYP2C19
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv948145
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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