A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642269



Internal ID7029039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:38997366..39005216hg38UCSC Ensembl
Innerchr18:38997395..39005188hg38UCSC Ensembl
Outerchr18:38997338..39005245hg38UCSC Ensembl
chr18:36577330..36585180hg19UCSC Ensembl
Innerchr18:36577359..36585152hg19UCSC Ensembl
Outerchr18:36577302..36585209hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg387851
hg197851
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15846596, essv15846604, essv15846602, essv15846606, essv15846598, essv15846597, essv15846603, essv15846600, essv15846605, essv15846599, essv15846601
SamplesHG03121, NA19914, HG02323, NA19201, HG02595, NA19235, HG03270, HG03571, HG02635, HG02558, NA19900
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642269
Frequency
Sample Size2504
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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