A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5473631



Internal ID251317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:16100953..16103921hg38UCSC Ensembl
chr5:16101062..16104030hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg382969
hg192969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16962828
Samples
Known GenesMARCH11
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5473631
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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