A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv981153



Internal ID18616352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:61567886..61577273hg38UCSC Ensembl
Innerchr6:62277791..62287178hg19UCSC Ensembl
Innerchr6:62335750..62345137hg18UCSC Ensembl
Cytoband6q11.1
Allele length
AssemblyAllele length
hg389388
hg199388
hg189388
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2412278, nssv2412283, nssv2412282, nssv2412275, nssv2412284, nssv2412277, nssv2412276, nssv2412280, nssv2412279, nssv2412281
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesMTRNR2L9
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv981153
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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