A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5900586



Internal ID9249727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:74032091..74081452hg38UCSC Ensembl
chr6:74741807..74791168hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3849362
hg1949362
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2657395
Supporting Variants
SamplesNA12046
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5900586
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer