A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6527571



Internal ID20900932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:73371878..73372365hg38UCSC Ensembl
chr18:71039113..71039600hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg38488
hg19488
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18045614
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6527571
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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