A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6453712



Internal ID9386722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:26167841..26171358hg38UCSC Ensembl
chr18:23747805..23751322hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg383518
hg193518
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag0
Merged StatusS
Merged Variantsesv2660254
Supporting Variants
SamplesNA18579
Known GenesPSMA8
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6453712
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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