A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970160



Internal ID18605384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:112355156..112362297hg38UCSC Ensembl
Innerchr6:112676358..112683499hg19UCSC Ensembl
Innerchr6:112783051..112790192hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg387142
hg197142
hg187142
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2420471, nssv2420475, nssv2420478, nssv2420474, nssv2420472, nssv2420476, nssv2420470, nssv2420469, nssv2420473, nssv2420477
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)nsv970160
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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