A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11659894



Internal ID648663
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3602800
Supporting Variants
SamplesHG00285
Known GenesPDGFC
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11659894
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer