A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6403793



Internal ID21061346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:95141375..95144547hg38UCSC Ensembl
chr5:94477079..94480251hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg383173
hg193173
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18135600
Samples
Known GenesMCTP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6403793
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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