A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv956e199



Internal ID11593215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:73399901..73404263hg38UCSC Ensembl
chr4:74265618..74269980hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg384363
hg194363
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2658250, esv2667927
SamplesHG00324
Known GenesALB
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv956e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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