A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6509175



Internal ID20882482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:82732195..82732579hg38UCSC Ensembl
chr16:82765800..82766184hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg38385
hg19385
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18032699
Samples
Known GenesCDH13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6509175
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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