A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3602766



Internal ID6643022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:155675673..155690759hg38UCSC Ensembl
Innerchr4:155675673..155690759hg38UCSC Ensembl
Outerchr4:155675173..155691259hg38UCSC Ensembl
chr4:156596825..156611911hg19UCSC Ensembl
Innerchr4:156596825..156611911hg19UCSC Ensembl
Outerchr4:156596325..156612411hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3815087
hg1915087
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11659347
SamplesNA18966
Known GenesGUCY1A3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3602766
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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