A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6512862



Internal ID20886202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:12669928..12869214hg38UCSC Ensembl
chr16:12763785..12963071hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg38199287
hg19199287
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18028719
Samples
Known GenesCPPED1, MIR4718
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6512862
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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