A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15937337



Internal ID5939153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:76213391..76437604hg38UCSC Ensembl
chr18:73925346..74149560hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38224214
hg19224215
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3643163
Supporting Variants
SamplesNA06984
Known GenesZNF516
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15937337
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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