A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3600217



Internal ID6640481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:36111290..36503831hg38UCSC Ensembl
Innerchr4:36111321..36503801hg38UCSC Ensembl
Outerchr4:36111260..36503862hg38UCSC Ensembl
chr4:36112912..36505453hg19UCSC Ensembl
Innerchr4:36112943..36505423hg19UCSC Ensembl
Outerchr4:36112882..36505484hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg38392542
hg19392542
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11394761
SamplesNA21129
Known GenesARAP2, DTHD1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3600217
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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