A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv946867



Internal ID18593717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:145291967..145292673hg38UCSC Ensembl
Innerchr1:148252237..148253022hg19UCSC Ensembl
Innerchr1:146618861..146619646hg18UCSC Ensembl
Cytoband1q21.1
Allele length
AssemblyAllele length
hg38707
hg19786
hg18786
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2593191, nssv2593226, nssv2593194, nssv2593229, nssv2593195, nssv2593196, nssv2593192, nssv2593231, nssv2593232, nssv2593193, nssv2593200, nssv2593197, nssv2593227, nssv2593198, nssv2593224, nssv2593228, nssv2593233, nssv2593225, nssv2593230, nssv2593199
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)nsv946867
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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