A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15934202



Internal ID3425612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:74817638..74827890hg38UCSC Ensembl
Innerchr18:74817638..74827890hg38UCSC Ensembl
Outerchr18:74817490..74828028hg38UCSC Ensembl
chr18:72529594..72539846hg19UCSC Ensembl
Innerchr18:72529594..72539846hg19UCSC Ensembl
Outerchr18:72529446..72539984hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3810253
hg1910253
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3643129
Supporting Variants
SamplesHG03061
Known GenesZNF407
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15934202
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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