A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11659718



Internal ID2648209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:156311917..156382716hg38UCSC Ensembl
Innerchr4:156311934..156382700hg38UCSC Ensembl
Outerchr4:156311901..156382733hg38UCSC Ensembl
chr4:157233069..157303868hg19UCSC Ensembl
Innerchr4:157233086..157303852hg19UCSC Ensembl
Outerchr4:157233053..157303885hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3870800
hg1970800
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3602778
Supporting Variants
SamplesHG02343
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11659718
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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