A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6488275



Internal ID21145828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:91408333..91650230hg38UCSC Ensembl
chr13:92060587..92302484hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg38241898
hg19241898
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18014668
Samples
Known GenesGPC5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6488275
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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