A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18060153



Internal ID20627193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:247344750..247362600hg38UCSC Ensembl
chr1:247508052..247525902hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg3817851
hg1917851
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6322130
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18060153
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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