A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18052249



Internal ID20619289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:156037354..156038134hg38UCSC Ensembl
chr1:156007145..156007925hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg38781
hg19781
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6319037
Supporting Variants
Samples
Known GenesMIR7851, UBQLN4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18052249
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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