A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18201098



Internal ID20768138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:178341154..178353144hg38UCSC Ensembl
chr1:178310289..178322279hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg3811991
hg1911991
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6322503
Supporting Variants
Samples
Known GenesRASAL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18201098
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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