A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17549898



Internal ID21874253
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:95230201..95230255hg38UCSC Ensembl
chr5:94565905..94565959hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6014124
Supporting Variants
Samples
Known GenesMCTP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17549898
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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