A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18014691



Internal ID20581731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:91615401..91617100hg38UCSC Ensembl
chr13:92267655..92269354hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6480386
Supporting Variants
Samples
Known GenesGPC5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18014691
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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