A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6505349



Internal ID20878618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:56494823..56501098hg38UCSC Ensembl
chr16:56528735..56535010hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg386276
hg196276
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18030224
Samples
Known GenesBBS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6505349
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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