A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15910004



Internal ID4682374
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:65787801..65798246hg38UCSC Ensembl
Innerchr18:65787801..65798246hg38UCSC Ensembl
Outerchr18:65787534..65798563hg38UCSC Ensembl
chr18:63455037..63465482hg19UCSC Ensembl
Innerchr18:63455037..63465482hg19UCSC Ensembl
Outerchr18:63454770..63465799hg19UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg3810446
hg1910446
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3642844
Supporting Variants
SamplesHG04209
Known GenesCDH7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15910004
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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