A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18128697



Internal ID20695737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:151330497..151334787hg38UCSC Ensembl
chr5:150710058..150714348hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg384291
hg194291
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6411072
Supporting Variants
Samples
Known GenesSLC36A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18128697
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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