A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642776



Internal ID6682856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:63638301..63656397hg38UCSC Ensembl
Innerchr18:63638801..63655897hg38UCSC Ensembl
Outerchr18:63637301..63657397hg38UCSC Ensembl
chr18:61305535..61323631hg19UCSC Ensembl
Innerchr18:61306035..61323131hg19UCSC Ensembl
Outerchr18:61304535..61324631hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg3818097
hg1918097
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv621e214
Supporting Variantsessv15906715, essv15906716, essv15906717
SamplesNA18977, HG03078, HG03367
Known GenesSERPINB3, SERPINB4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642776
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer