A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975702



Internal ID18264223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:50003319..50009992hg38UCSC Ensembl
Innerchr10:51763079..51769752hg19UCSC Ensembl
Innerchr10:51433085..51439758hg18UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg386674
hg196674
hg186674
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2614489, nssv2614485, nssv2614483, nssv2614488, nssv2614484, nssv2614490, nssv2614482, nssv2614491, nssv2614487, nssv2614486
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesAGAP6
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975702
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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