A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17545376



Internal ID21869731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:95228591..95228591hg38UCSC Ensembl
chr5:94564295..94564295hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6077419
Supporting Variants
Samples
Known GenesMCTP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17545376
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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