A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv978603



Internal ID18613806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:12039959..12046832hg38UCSC Ensembl
Innerchr18:12039958..12046831hg19UCSC Ensembl
Innerchr18:12029958..12036831hg18UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg386874
hg196874
hg186874
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2115199, nssv2115201, nssv2115193, nssv2115197, nssv2115200, nssv2115192, nssv2115194, nssv2115195, nssv2115198, nssv2115196
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)nsv978603
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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