A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6208587



Internal ID9053431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:83012803..83018574hg38UCSC Ensembl
chr17:80970679..80976450hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg385772
hg195772
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2668880
Supporting Variants
SamplesHG00699
Known GenesB3GNTL1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6208587
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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