A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18128225



Internal ID20695265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:21832701..21839100hg38UCSC Ensembl
chr5:21832810..21839209hg19UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg386400
hg196400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6384759
Supporting Variants
Samples
Known GenesCDH12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18128225
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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