A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv960416



Internal ID18595667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:14233017..14238718hg38UCSC Ensembl
Innerchr17:14136334..14142035hg19UCSC Ensembl
Innerchr17:14077059..14082760hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg385702
hg195702
hg185702
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2077938, nssv2077939, nssv2077944, nssv2077945, nssv2077941, nssv2077937, nssv2077943, nssv2077940, nssv2077942, nssv2077936
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesCDRT15
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv960416
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