A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11397806



Internal ID2913759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:38716022..38718684hg38UCSC Ensembl
Innerchr4:38716072..38718634hg38UCSC Ensembl
Outerchr4:38715972..38718734hg38UCSC Ensembl
chr4:38717643..38720305hg19UCSC Ensembl
Innerchr4:38717693..38720255hg19UCSC Ensembl
Outerchr4:38717593..38720355hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg382663
hg192663
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3600263
Supporting Variants
SamplesHG02580
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11397806
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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