A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18032357



Internal ID20599397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:82844170..82854577hg38UCSC Ensembl
chr16:82877775..82888182hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3810408
hg1910408
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6503083
Supporting Variants
Samples
Known GenesCDH13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18032357
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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