A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18179815



Internal ID20746855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:87800101..87818700hg38UCSC Ensembl
chr13:88452356..88470955hg19UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg3818600
hg1918600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6480356
Supporting Variants
Samples
Known GenesLINC00397
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18179815
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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