A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18129810



Internal ID20696850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:35934927..35942114hg38UCSC Ensembl
chr5:35935029..35942216hg19UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg387188
hg197188
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6378493
Supporting Variants
Samples
Known GenesCAPSL, LOC100506406
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18129810
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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