A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18071574



Internal ID20638614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:42024536..42027184hg38UCSC Ensembl
chr21:43444645..43447293hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg382649
hg192649
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6536914
Supporting Variants
Samples
Known GenesZNF295-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18071574
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00018


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