A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6531500



Internal ID20904861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:31134114..31134703hg38UCSC Ensembl
chr18:28714077..28714666hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg38590
hg19590
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18039896
Samples
Known GenesDSC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6531500
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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