A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6392847



Internal ID9370250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:136261477..136268161hg38UCSC Ensembl
chr6:136582615..136589299hg19UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg386685
hg196685
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag0
Merged StatusS
Merged Variantsesv2673118
Supporting Variants
SamplesNA19719
Known GenesBCLAF1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6392847
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