A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981207



Internal ID18616406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167165853..167178336hg38UCSC Ensembl
Innerchr6:167579341..167591824hg19UCSC Ensembl
Innerchr6:167499331..167511814hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3812484
hg1912484
hg1812484
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2431517, nssv2431522, nssv2431523, nssv2431514, nssv2431516, nssv2431519, nssv2431518, nssv2431515, nssv2431520, nssv2431521
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesTCP10L2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv981207
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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