A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11659914



Internal ID4183200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:157242916..157302129hg38UCSC Ensembl
chr4:158164068..158223281hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3859214
hg1959214
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3602807
Supporting Variants
SamplesHG03777
Known GenesGRIA2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11659914
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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