A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18137030



Internal ID20704070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:109122900..109229299hg38UCSC Ensembl
chr6:109444103..109550502hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38106400
hg19106400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6601517
Supporting Variants
Samples
Known GenesCEP57L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18137030
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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