A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11633052



Internal ID1634868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:139692926..139951592hg38UCSC Ensembl
chr4:140614080..140872746hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg38258667
hg19258667
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3602439
Supporting Variants
SamplesHG03914
Known GenesMAML3, MGST2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11633052
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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