A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv969415



Internal ID18604642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:63613846..63616405hg38UCSC Ensembl
Innerchr6:64323751..64326310hg19UCSC Ensembl
Innerchr6:64381710..64384269hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg382560
hg192560
hg182560
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2415282, nssv2415278, nssv2415281, nssv2415279, nssv2415285, nssv2415287, nssv2415286, nssv2415283, nssv2415284, nssv2415280
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv969415
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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