A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3602794



Internal ID6989827
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11659886
SamplesHG02180
Known GenesPDGFC
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3602794
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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