A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv958e199



Internal ID20124260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:76203140..76205259hg38UCSC Ensembl
chr4:77124293..77126412hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg382120
hg192120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2665048, esv2671343
SamplesNA18628
Known GenesSCARB2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv958e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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