A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv966311



Internal ID18254855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:113213323..113214921hg38UCSC Ensembl
Innerchr4:114134479..114136077hg19UCSC Ensembl
Innerchr4:114353928..114355526hg18UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg381599
hg191599
hg181599
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2332883, nssv2332877, nssv2332879, nssv2332886, nssv2332884, nssv2332880, nssv2332885, nssv2332881, nssv2332882, nssv2332878
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesANK2
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv966311
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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