A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6141725



Internal ID9656988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:82970519..82970656hg38UCSC Ensembl
chr17:80928395..80928532hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38138
hg19138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2656462
Supporting Variants
SamplesNA19390
Known GenesB3GNTL1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6141725
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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