A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4731718



Internal ID20507639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:94953858..94953928hg38UCSC Ensembl
chr5:94289562..94289632hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16267875
Samples
Known GenesMCTP1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4731718
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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