A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv946949



Internal ID18247113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:148574927..148576707hg38UCSC Ensembl
Innerchr1:148311496..148313462hg19UCSC Ensembl
Innerchr1:146678120..146680086hg18UCSC Ensembl
Cytoband1q21.1
Allele length
AssemblyAllele length
hg381781
hg191967
hg181967
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2598875, nssv2598883, nssv2598882, nssv2598880, nssv2598878, nssv2598879, nssv2598884, nssv2598881, nssv2598877, nssv2598876
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)nsv946949
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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