A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv963059



Internal ID18598301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:44117586..44118561hg38UCSC Ensembl
Innerchr19:44621739..44622714hg19UCSC Ensembl
Innerchr19:49313579..49314554hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38976
hg19976
hg18976
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2152627, nssv2152629, nssv2152630, nssv2152625, nssv2152621, nssv2152628, nssv2152622, nssv2152623, nssv2152626, nssv2152624
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesZNF225
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv963059
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