A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18052137



Internal ID20619177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:146000277..146011372hg38UCSC Ensembl
chr1:145423637..145434783hg19UCSC Ensembl
Cytoband1q21.1
Allele length
AssemblyAllele length
hg3811096
hg1911147
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6325562
Supporting Variants
Samples
Known GenesLOC100288142, NBPF10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18052137
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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