A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv980202



Internal ID18615402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:49486925..49492597hg38UCSC Ensembl
Innerchr4:49488942..49494614hg19UCSC Ensembl
Innerchr4:49183599..49189371hg18UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg385673
hg195673
hg185773
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2693841, nssv2693839, nssv2693840, nssv2693832, nssv2693837, nssv2693838, nssv2693834, nssv2693833, nssv2693835, nssv2693836
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv980202
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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