A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948143



Internal ID18594989
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:93958006..93961662hg38UCSC Ensembl
Innerchr10:95717763..95721419hg19UCSC Ensembl
Innerchr10:95707753..95711409hg18UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg383657
hg193657
hg183657
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1866050, nssv1866044, nssv1866046, nssv1866043, nssv1866045, nssv1866047, nssv1866051, nssv1866042, nssv1866048, nssv1866049
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesPIPSL
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv948143
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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