A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6519997



Internal ID20893358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:75429276..75429867hg38UCSC Ensembl
chr18:73141231..73141822hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38592
hg19592
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18044031
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6519997
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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