A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3602541



Internal ID6989575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:144412375..144433455hg38UCSC Ensembl
Innerchr4:144412400..144433430hg38UCSC Ensembl
Outerchr4:144412350..144433480hg38UCSC Ensembl
chr4:145333527..145354607hg19UCSC Ensembl
Innerchr4:145333552..145354582hg19UCSC Ensembl
Outerchr4:145333502..145354632hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg3821081
hg1921081
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11639967, essv11639969, essv11639971, essv11639968, essv11639970
SamplesHG01795, HG01860, HG02395, HG00531, HG00620
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3602541
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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