A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3600790



Internal ID6987830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:65303810..65313708hg38UCSC Ensembl
Innerchr4:65303810..65313708hg38UCSC Ensembl
Outerchr4:65303552..65313953hg38UCSC Ensembl
chr4:66169528..66179426hg19UCSC Ensembl
Innerchr4:66169528..66179426hg19UCSC Ensembl
Outerchr4:66169270..66179671hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg389899
hg199899
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11469237, essv11469236
SamplesHG01070, HG01197
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3600790
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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