A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv945595



Internal ID18592446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:121398461..121407875hg38UCSC Ensembl
Innerchr1:121140321..121149735hg19UCSC Ensembl
Innerchr1:120841844..120851258hg18UCSC Ensembl
Cytoband1p11.2
Allele length
AssemblyAllele length
hg389415
hg199415
hg189415
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2574130, nssv2574135, nssv2574127, nssv2574134, nssv2574133, nssv2574131, nssv2574129, nssv2574126, nssv2574128, nssv2574132
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known Genes
MethodSequencing
Analysislineage specific fixed expansions
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv945595
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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