A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv975e214



Internal ID22756869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:7795564..7797447hg38UCSC Ensembl
chr4:7797291..7799174hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg381884
hg191884
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3599536, esv3599537
SamplesHG01052, NA11893
Known GenesAFAP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv975e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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