A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11463400



Internal ID1014704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:64342926..64472027hg38UCSC Ensembl
Innerchr4:64342926..64472027hg38UCSC Ensembl
Outerchr4:64342426..64472527hg38UCSC Ensembl
chr4:65208644..65337745hg19UCSC Ensembl
Innerchr4:65208644..65337745hg19UCSC Ensembl
Outerchr4:65208144..65338245hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg38129102
hg19129102
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3600764
Supporting Variants
SamplesHG00634
Known GenesTECRL
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11463400
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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