A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3569600



Internal ID6694296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:136276508..136277863hg38UCSC Ensembl
chr6:136597646..136599001hg19UCSC Ensembl
chr6:136639339..136640694hg18UCSC Ensembl
Cytoband6q23.3
Allele length
AssemblyAllele length
hg381356
hg191356
hg181356
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv990963
Supporting Variants
SamplesHuRef
Known GenesBCLAF1
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3569600
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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