A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948210



Internal ID18595056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:122592000..122619400hg38UCSC Ensembl
Innerchr10:124351516..124378916hg19UCSC Ensembl
Innerchr10:124341506..124368906hg18UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3827401
hg1927401
hg1827401
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1870120, nssv1870115, nssv1870114, nssv1870116, nssv1870121, nssv1870118, nssv1870119, nssv1870117, nssv1870113, nssv1870112
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesDMBT1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv948210
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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