A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975705



Internal ID18610912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:73681394..73682009hg38UCSC Ensembl
Innerchr10:75441152..75441767hg19UCSC Ensembl
Innerchr10:75111158..75111773hg18UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38616
hg19616
hg18616
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2615786, nssv2615791, nssv2615788, nssv2615790, nssv2615789, nssv2615784, nssv2615787, nssv2615785, nssv2615792, nssv2615783
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesAGAP5
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975705
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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