A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv970113



Internal ID18258651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:42207002..42208692hg38UCSC Ensembl
Innerchr6:42174740..42176430hg19UCSC Ensembl
Innerchr6:42282718..42284408hg18UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg381691
hg191691
hg181691
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2408802, nssv2408808, nssv2408807, nssv2408805, nssv2408806, nssv2408804, nssv2408803, nssv2408810, nssv2408811, nssv2408809
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesMRPS10
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv970113
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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