A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18215948



Internal ID20782988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:16174701..16183200hg38UCSC Ensembl
chr5:16174810..16183309hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg388500
hg198500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6385929
Supporting Variants
Samples
Known GenesMARCH11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18215948
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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