A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6481093



Internal ID21138646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:92012727..92065863hg38UCSC Ensembl
chr13:92664980..92718116hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3853137
hg1953137
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18016335
Samples
Known GenesGPC5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6481093
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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