A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv946897



Internal ID18247061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:148544667..148547259hg38UCSC Ensembl
Innerchr1:148269992..148272606hg19UCSC Ensembl
Innerchr1:146636616..146639230hg18UCSC Ensembl
Cytoband1q21.1
Allele length
AssemblyAllele length
hg382593
hg192615
hg182615
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv13n82
Supporting Variantsnssv2595628, nssv2595632, nssv2595629, nssv2595627, nssv2595633, nssv2595626, nssv2595630, nssv2595635, nssv2595631, nssv2595634
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)nsv946897
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