A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642655



Internal ID7029424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:58869981..58872955hg38UCSC Ensembl
Innerchr18:58869981..58872955hg38UCSC Ensembl
Outerchr18:58869706..58873159hg38UCSC Ensembl
chr18:56537213..56540187hg19UCSC Ensembl
Innerchr18:56537213..56540187hg19UCSC Ensembl
Outerchr18:56536938..56540391hg19UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg382975
hg192975
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15894283
SamplesNA19225
Known GenesZNF532
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642655
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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