A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv960103



Internal ID18595356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:41369437..41370086hg38UCSC Ensembl
Innerchr17:39525689..39526338hg19UCSC Ensembl
Innerchr17:36779215..36779864hg18UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg38650
hg19650
hg18650
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2095922, nssv2095929, nssv2095928, nssv2095923, nssv2095927, nssv2095926, nssv2095930, nssv2095924, nssv2095925, nssv2095921
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesKRT33B
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv960103
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