A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3602800



Internal ID6989833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:156957024..156959368hg38UCSC Ensembl
Innerchr4:156957062..156959331hg38UCSC Ensembl
Outerchr4:156956987..156959406hg38UCSC Ensembl
chr4:157878176..157880520hg19UCSC Ensembl
Innerchr4:157878214..157880483hg19UCSC Ensembl
Outerchr4:157878139..157880558hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg382345
hg192345
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11659894, essv11659895
SamplesHG00328, HG00285
Known GenesPDGFC
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3602800
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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