A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv956e199



Internal ID6312060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:74265618..74269980hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg19n/a
Variant TypeCNV Deletion
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsesv2658250, esv2667927
SamplesHG00324
Known GenesALB
Method
Analysis
Platform
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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