A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5902556



Internal ID22677715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:94803617..94806545hg38UCSC Ensembl
chr5:94139322..94142250hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg382929
hg192929
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17420660
Samples
Known GenesMCTP1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5902556
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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