A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv980209



Internal ID18615409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:66093805..66095248hg38UCSC Ensembl
Innerchr4:66959523..66960966hg19UCSC Ensembl
Innerchr4:66642118..66643561hg18UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg381444
hg191444
hg181444
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2320903, nssv2320901, nssv2320902, nssv2320899, nssv2320904, nssv2320905, nssv2320900, nssv2320908, nssv2320906, nssv2320907
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)nsv980209
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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