A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18033970



Internal ID20601010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:9809247..9819775hg38UCSC Ensembl
chr16:9903104..9913632hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3810529
hg1910529
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6495792
Supporting Variants
Samples
Known GenesGRIN2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18033970
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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