A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965750



Internal ID18254294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:110704761..110708383hg38UCSC Ensembl
Innerchr6:111025964..111029586hg19UCSC Ensembl
Innerchr6:111132657..111136279hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg383623
hg193623
hg183623
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2419230, nssv2419231, nssv2419229, nssv2419236, nssv2419234, nssv2419235, nssv2419238, nssv2419233, nssv2419237, nssv2419232
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCDK19
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv965750
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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