A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18061626



Internal ID20628666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:47886895..47887587hg38UCSC Ensembl
chr1:48352567..48353259hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg38693
hg19693
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6316335
Supporting Variants
Samples
Known GenesTRABD2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18061626
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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