A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv946933



Internal ID18247097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:148565164..148565912hg38UCSC Ensembl
Innerchr1:148300287..148301035hg19UCSC Ensembl
Innerchr1:146666911..146667659hg18UCSC Ensembl
Cytoband1q21.1
Allele length
AssemblyAllele length
hg38749
hg19749
hg18749
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2598319, nssv2598321, nssv2598317, nssv2598318, nssv2598323, nssv2598316, nssv2598322, nssv2598320, nssv2598324, nssv2598315
SamplesHGDP00927, HGDP00778, HGDP00542, HGDP01029, HGDP01284, HGDP00521, HGDP00998, HGDP00456, HGDP01307, HGDP00665
Known GenesLOC101929780, NBPF10, NBPF14, NBPF8, NBPF9
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv946933
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