A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18061227



Internal ID20628267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:38158027..38160985hg38UCSC Ensembl
chr1:38623699..38626657hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg382959
hg192959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6329428
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18061227
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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