A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975708



Internal ID18610915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:87007642..87009775hg38UCSC Ensembl
Innerchr10:88767399..88769532hg19UCSC Ensembl
Innerchr10:88757379..88759512hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg382134
hg192134
hg182134
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2616221, nssv2616225, nssv2616230, nssv2616229, nssv2616224, nssv2616222, nssv2616227, nssv2616223, nssv2616226, nssv2616228
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesAGAP11
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975708
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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