A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv946889



Internal ID18247053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:148541431..148542179hg38UCSC Ensembl
Innerchr1:148266718..148267466hg19UCSC Ensembl
Innerchr1:146633342..146634090hg18UCSC 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 Variantsnssv2593872, nssv2594373, nssv2594316, nssv2594378, nssv2594322, nssv2594375, nssv2594315, nssv2594380, nssv2594372, nssv2594323, nssv2594314, nssv2594376, nssv2594377, nssv2594374, nssv2594320, nssv2594379, nssv2594321, nssv2594318, nssv2594317, nssv2594319
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesLOC101929780, NBPF10, NBPF14, NBPF8, NBPF9
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv946889
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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