A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18066151



Internal ID20633191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:99280046..99280653hg38UCSC Ensembl
chr1:99745602..99746209hg19UCSC Ensembl
Cytoband1p21.2
Allele length
AssemblyAllele length
hg38608
hg19608
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6329104
Supporting Variants
Samples
Known GenesLPPR4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18066151
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00056


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