A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11741602



Internal ID1743418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:185579224..185611747hg38UCSC Ensembl
chr4:186500378..186532901hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3832524
hg1932524
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3603509
Supporting Variants
SamplesHG03224
Known GenesSORBS2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11741602
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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