A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv982770



Internal ID18271279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:50002819..50003319hg38UCSC Ensembl
Innerchr10:51762579..51763079hg19UCSC Ensembl
Innerchr10:51432585..51433085hg18UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg38501
hg19501
hg18501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2613177, nssv2613170, nssv2613178, nssv2613173, nssv2613172, nssv2613175, nssv2613171, nssv2613174, nssv2613176, nssv2613169
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesAGAP6
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv982770
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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