A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv969358



Internal ID18604585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:26420161..26423289hg38UCSC Ensembl
Innerchr6:26420389..26423517hg19UCSC Ensembl
Innerchr6:26528368..26531496hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg383129
hg193129
hg183129
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2397058, nssv2397055, nssv2397059, nssv2397060, nssv2397056, nssv2397063, nssv2397062, nssv2397057, nssv2397061, nssv2397054
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesBTN2A3P
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv969358
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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