A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv979863



Internal ID18615064
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:106109292..106113255hg38UCSC Ensembl
Innerchr3:105828139..105832102hg19UCSC Ensembl
Innerchr3:107310829..107314792hg18UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg383964
hg193964
hg183964
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2292896, nssv2292904, nssv2292895, nssv2292897, nssv2292903, nssv2292899, nssv2292900, nssv2292898, nssv2292902, nssv2292901
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)nsv979863
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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