A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11659886



Internal ID2471314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:156882145..156905163hg38UCSC Ensembl
Innerchr4:156882145..156905163hg38UCSC Ensembl
Outerchr4:156881645..156905663hg38UCSC Ensembl
chr4:157803297..157826315hg19UCSC Ensembl
Innerchr4:157803297..157826315hg19UCSC Ensembl
Outerchr4:157802797..157826815hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3823019
hg1923019
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3602794
Supporting Variants
SamplesHG02180
Known GenesPDGFC
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11659886
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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