A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18052083



Internal ID20619123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:155576440..155578408hg38UCSC Ensembl
chr1:155546231..155548199hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg381969
hg191969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6331700
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18052083
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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