A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6328050



Internal ID20861195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9810694..9813134hg38UCSC Ensembl
chr1:9870752..9873192hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg382441
hg192441
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18065229
Samples
Known GenesCLSTN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6328050
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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