A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18061691



Internal ID20628731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:56050645..56053554hg38UCSC Ensembl
chr1:56516318..56519227hg19UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg382910
hg192910
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6327866
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18061691
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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