A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642775



Internal ID6682855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:63635738..63653861hg38UCSC Ensembl
Innerchr18:63635888..63653711hg38UCSC Ensembl
Outerchr18:63635588..63654011hg38UCSC Ensembl
chr18:61302972..61321095hg19UCSC Ensembl
Innerchr18:61303122..61320945hg19UCSC Ensembl
Outerchr18:61302822..61321245hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg3818124
hg1918124
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv621e214
Supporting Variantsessv15906714, essv15906713
SamplesHG03078, HG03367
Known GenesSERPINB4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642775
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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