A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982768



Internal ID18617963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46108645..46113017hg38UCSC Ensembl
Innerchr10:51482805..51487177hg19UCSC Ensembl
Innerchr10:51152811..51157183hg18UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg384373
hg194373
hg184373
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2614285, nssv2614292, nssv2614288, nssv2614287, nssv2614284, nssv2614291, nssv2614286, nssv2614289, nssv2614290, nssv2614293
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesAGAP7
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982768
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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