A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6014117



Internal ID21923460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:95172170..95209773hg38UCSC Ensembl
chr5:94507874..94545477hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3837604
hg1937604
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17550531
Samples
Known GenesMCTP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6014117
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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