A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18013227



Internal ID20580267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:77746142..77746743hg38UCSC Ensembl
chr13:78320277..78320878hg19UCSC Ensembl
Cytoband13q22.3
Allele length
AssemblyAllele length
hg38602
hg19602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6493096
Supporting Variants
Samples
Known GenesSLAIN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18013227
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00021


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