A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18043434



Internal ID20610474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:63759834..63763369hg38UCSC Ensembl
chr18:61427068..61430603hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg383536
hg193536
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6534130
Supporting Variants
Samples
Known GenesSERPINB7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18043434
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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