A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18054405



Internal ID20621446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:184074573..184075043hg38UCSC Ensembl
chr1:184043707..184044177hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg38471
hg19471
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6325427
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18054405
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00037


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