A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11394762



Internal ID6947521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:36111466..36183939hg38UCSC Ensembl
chr4:36113088..36185561hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3872474
hg1972474
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3600218
Supporting Variants
SamplesNA21129
Known GenesARAP2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11394762
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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