A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18052275



Internal ID20619315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:15661418..15661903hg38UCSC Ensembl
chr1:15987913..15988398hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg38486
hg19486
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6329858
Supporting Variants
Samples
Known GenesRSC1A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18052275
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0004


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