A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11465395



Internal ID2550251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:64777236..64780933hg38UCSC Ensembl
Innerchr4:64777266..64780903hg38UCSC Ensembl
Outerchr4:64777206..64780963hg38UCSC Ensembl
chr4:65642954..65646651hg19UCSC Ensembl
Innerchr4:65642984..65646621hg19UCSC Ensembl
Outerchr4:65642924..65646681hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg383698
hg193698
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3600770
Supporting Variants
SamplesHG02265
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11465395
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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