A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv665e214



Internal ID20122088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:46134382..46255762hg38UCSC Ensembl
chr19:46637639..46759019hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg38121381
hg19121381
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3644522, esv3644521
SamplesHG01860, HG01187, HG00478
Known GenesDKFZp434J0226, IGFL1, IGFL2, RNU6-66P
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv665e214
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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