A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18065964



Internal ID20633004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:98989617..98993649hg38UCSC Ensembl
chr1:99455173..99459205hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg384033
hg194033
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6316774
Supporting Variants
Samples
Known GenesLPPR5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18065964
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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