A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18061155



Internal ID20628195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:36410097..36411937hg38UCSC Ensembl
chr1:36875698..36877538hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg381841
hg191841
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6330665
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18061155
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00016


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