A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6487734



Internal ID21145287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:51358491..51358922hg38UCSC Ensembl
chr13:51932627..51933058hg19UCSC Ensembl
Cytoband13q14.3
Allele length
AssemblyAllele length
hg38432
hg19432
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18009664
Samples
Known GenesSERPINE3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6487734
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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