A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv664e214



Internal ID22756558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:44606502..44610197hg38UCSC Ensembl
chr19:45109819..45113515hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg383696
hg193697
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3644489, esv3644490
SamplesNA19023, HG02255, NA19108
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv664e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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