A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5750941



Internal ID8742101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:97433139..97438062hg38UCSC Ensembl
chr4:98354290..98359213hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg384924
hg194924
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2657643
Supporting Variants
SamplesHG00131
Known GenesSTPG2-AS1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5750941
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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