A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975884



Internal ID18264405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:11352691..11353287hg38UCSC Ensembl
Innerchr11:11374238..11374834hg19UCSC Ensembl
Innerchr11:11330814..11331410hg18UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg38597
hg19597
hg18597
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1877521, nssv1877517, nssv1877520, nssv1877516, nssv1877522, nssv1877515, nssv1877514, nssv1877523, nssv1877518, nssv1877519
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesCSNK2A3, GALNT18
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975884
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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