A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv980218



Internal ID18615418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:73026219..73028228hg38UCSC Ensembl
Innerchr4:73891936..73893945hg19UCSC Ensembl
Innerchr4:74110800..74112809hg18UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg382010
hg192010
hg182010
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2323081, nssv2323080, nssv2323078, nssv2323075, nssv2323072, nssv2323073, nssv2323079, nssv2323076, nssv2323077, nssv2323074
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)nsv980218
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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