A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv947440



Internal ID18594288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:107066111..107078609hg38UCSC Ensembl
Innerchr1:107608733..107621231hg19UCSC Ensembl
Innerchr1:107410256..107422754hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3812499
hg1912499
hg1812499
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2763319
SamplesHGDP00998
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv947440
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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