A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv972062



Internal ID18260592
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:93729609..93730453hg38UCSC Ensembl
Innerchr11:93462775..93463619hg19UCSC Ensembl
Innerchr11:93102423..93103267hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38845
hg19845
hg18845
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1901347, nssv1901352, nssv1901349, nssv1901345, nssv1901350, nssv1901351, nssv1901348, nssv1901343, nssv1901344, nssv1901346
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesKIAA1731
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv972062
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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