A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv978770



Internal ID18613973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:9820104..9821620hg38UCSC Ensembl
Innerchr19:9930780..9932296hg19UCSC Ensembl
Innerchr19:9791780..9793296hg18UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381517
hg191517
hg181517
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2131446, nssv2131440, nssv2131444, nssv2131441, nssv2131437, nssv2131443, nssv2131445, nssv2131439, nssv2131438, nssv2131442
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)nsv978770
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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