A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947428



Internal ID18594276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:51049392..51077656hg38UCSC Ensembl
Innerchr1:51515064..51543328hg19UCSC Ensembl
Innerchr1:51287652..51315916hg18UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg3828265
hg1928265
hg1828265
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2758150
SamplesHGDP00998
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv947428
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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