A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11659896



Internal ID1661712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:156958946..157162701hg38UCSC Ensembl
chr4:157880098..158083853hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38203756
hg19203756
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3602801
Supporting Variants
SamplesNA18610
Known GenesGLRB, PDGFC
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11659896
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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