A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18177362



Internal ID20744402
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113075976..113108891hg38UCSC Ensembl
chr13:113730290..113763205hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3832916
hg1932916
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6484993
Supporting Variants
Samples
Known GenesF7, MCF2L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18177362
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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