A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1043e214



Internal ID22756937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:174496669..174512584hg38UCSC Ensembl
chr4:175417820..175433735hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg3815916
hg1915916
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3603229, esv3603230
SamplesHG02561, HG01308
Known GenesHPGD
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1043e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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