A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965743



Internal ID18600973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:87068667..87070879hg38UCSC Ensembl
Innerchr6:87778385..87780597hg19UCSC Ensembl
Innerchr6:87835104..87837316hg18UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg382213
hg192213
hg182213
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2417001, nssv2416996, nssv2416998, nssv2417002, nssv2417003, nssv2416995, nssv2416999, nssv2416997, nssv2417000, nssv2416994
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)nsv965743
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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