A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18029315



Internal ID20596355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:28177922..28179891hg38UCSC Ensembl
chr16:28189243..28191212hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381970
hg191970
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6513731
Supporting Variants
Samples
Known GenesXPO6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18029315
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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