A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532632



Internal ID20905993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:63634465..63652395hg38UCSC Ensembl
chr18:61301699..61319629hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg3817931
hg1917931
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3389n223
Supporting Variantsnssv18043413
Samples
Known GenesSERPINB4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532632
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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