A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6529885



Internal ID20903246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:37605989..37614956hg38UCSC Ensembl
chr18:35185952..35194919hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg388968
hg198968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18040447
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6529885
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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