A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18060997



Internal ID20628037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:34174283..34176594hg38UCSC Ensembl
chr1:34639884..34642195hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg382312
hg192312
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6322725
Supporting Variants
Samples
Known GenesC1orf94
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18060997
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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