A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18189855



Internal ID20756895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:91512970..91517883hg38UCSC Ensembl
chr13:92165224..92170137hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg384914
hg194914
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6489830
Supporting Variants
Samples
Known GenesGPC5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18189855
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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