A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6544057



Internal ID9087378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:134833655..134838899hg38UCSC Ensembl
Outerchr6:134833618..134838949hg38UCSC Ensembl
Innerchr6:135154793..135160037hg19UCSC Ensembl
Outerchr6:135154756..135160087hg19UCSC Ensembl
Cytoband6q23.2
Allele length
AssemblyAllele length
hg385332
hg195332
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2658359
Supporting Variants
SamplesHG01069
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6544057
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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