A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2658250



Internal ID9577669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:73400200..73404110hg38UCSC Ensembl
Outerchr4:73400043..73404263hg38UCSC Ensembl
Innerchr4:74265917..74269827hg19UCSC Ensembl
Outerchr4:74265760..74269980hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg384221
hg194221
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv956e199
Supporting Variantsessv5803599
SamplesHG00324
Known GenesALB
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2658250
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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