A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5664280



Internal ID9652325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:150432387..150433928hg38UCSC Ensembl
Outerchr6:150432230..150434081hg38UCSC Ensembl
Innerchr6:150753523..150755064hg19UCSC Ensembl
Outerchr6:150753366..150755217hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg381852
hg191852
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2656667
Supporting Variants
SamplesNA19383
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5664280
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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