A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535066



Internal ID20908427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:13778452..13782438hg38UCSC Ensembl
chr18:13778451..13782437hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg383987
hg193987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18039233
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6535066
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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