A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18051698



Internal ID20618738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:115334240..115336391hg38UCSC Ensembl
chr1:115876861..115879012hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg382152
hg192152
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6324829
Supporting Variants
Samples
Known GenesNGF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18051698
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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