A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3601129



Internal ID6988168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:79935894..79966679hg38UCSC Ensembl
chr4:80857048..80887833hg19UCSC Ensembl
Cytoband4q21.21
Allele length
AssemblyAllele length
hg3830786
hg1930786
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1009e214
Supporting Variantsessv11516646, essv11516645
SamplesNA21092, HG02716
Known GenesANTXR2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3601129
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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