A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6532485



Internal ID20905846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:37624797..37625229hg38UCSC Ensembl
chr18:35204760..35205192hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38433
hg19433
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18040449
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6532485
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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