A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18062127



Internal ID20629167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:61194303..61195065hg38UCSC Ensembl
chr1:61659975..61660737hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38763
hg19763
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6335358
Supporting Variants
Samples
Known GenesNFIA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18062127
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00016


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