A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv946881



Internal ID18247045
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:148536161..148536821hg38UCSC Ensembl
Innerchr1:148261394..148262068hg19UCSC Ensembl
Innerchr1:146628018..146628692hg18UCSC Ensembl
Cytoband1q21.1
Allele length
AssemblyAllele length
hg38661
hg19675
hg18675
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2594844, nssv2594901, nssv2594842, nssv2594839, nssv2594837, nssv2594895, nssv2594838, nssv2594900, nssv2594898, nssv2594899, nssv2594845, nssv2594897, nssv2594896, nssv2594841, nssv2594843, nssv2594840, nssv2594903, nssv2594894, nssv2594836, nssv2594902
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)nsv946881
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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