A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18053776



Internal ID20620816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:177055601..177123500hg38UCSC Ensembl
chr1:177024737..177092636hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg3867900
hg1967900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6322458
Supporting Variants
Samples
Known GenesASTN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18053776
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00036


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