A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv965870



Internal ID18601100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:30335462..30417700hg38UCSC Ensembl
Innerchr20:29570138..29652376hg19UCSC Ensembl
Innerchr20:28183799..28266037hg18UCSC Ensembl
Cytoband20q11.1
Allele length
AssemblyAllele length
hg3882239
hg1982239
hg1882239
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2233996, nssv2233993, nssv2233988, nssv2233990, nssv2233987, nssv2233991, nssv2233994, nssv2233995, nssv2233992, nssv2233989
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesFRG1B, MLLT10P1
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv965870
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer