A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18062006



Internal ID20629046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:51671331..51671968hg38UCSC Ensembl
chr1:52137003..52137640hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg38638
hg19638
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6328407
Supporting Variants
Samples
Known GenesOSBPL9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18062006
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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