A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517897



Internal ID20891258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:9015010..9015613hg38UCSC Ensembl
chr18:9015008..9015611hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg38604
hg19604
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18044343
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517897
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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