A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18110236



Internal ID20677276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:148618968..148619427hg38UCSC Ensembl
chr4:149540120..149540579hg19UCSC Ensembl
Cytoband4q31.23
Allele length
AssemblyAllele length
hg38460
hg19460
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6391347
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18110236
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00138


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