A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18066089



Internal ID20633129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:95055657..95058317hg38UCSC Ensembl
chr1:95521213..95523873hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg382661
hg192661
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6322316
Supporting Variants
Samples
Known GenesALG14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18066089
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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