A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18054554



Internal ID20621595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:179926216..179926551hg38UCSC Ensembl
chr1:179895351..179895686hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg38336
hg19336
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6323342
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18054554
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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