A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6528574



Internal ID20901935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:31972401..31973900hg38UCSC Ensembl
chr18:29552364..29553863hg19UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3340n223
Supporting Variantsnssv18039952
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6528574
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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