A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18054070



Internal ID20621110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:178690501..178706000hg38UCSC Ensembl
chr1:178659636..178675135hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg3815500
hg1915500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6322716
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18054070
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00204


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