A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv948133



Internal ID18594979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:91052926..91056046hg38UCSC Ensembl
Innerchr10:92812683..92815803hg19UCSC Ensembl
Innerchr10:92802663..92805783hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg383121
hg193121
hg183121
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1862797, nssv1862800, nssv1862799, nssv1862798, nssv1862795, nssv1862801, nssv1862796, nssv1862793, nssv1862794, nssv1862802
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLINC00502
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv948133
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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