A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15934122



Internal ID4721888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:74701859..75054754hg38UCSC Ensembl
chr18:72413815..72766710hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg38352896
hg19352896
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3643125
Supporting Variants
SamplesNA06984
Known GenesZNF407
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15934122
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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