A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6521194



Internal ID20894555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:63637701..63655700hg38UCSC Ensembl
chr18:61304935..61322934hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg3818000
hg1918000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3389n223
Supporting Variantsnssv18043415
Samples
Known GenesSERPINB3, SERPINB4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6521194
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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