A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6361426



Internal ID21018979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:25145456..25147058hg38UCSC Ensembl
chr4:25147078..25148680hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg381603
hg191603
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18113392
Samples
Known GenesSEPSECS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6361426
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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