A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6507224



Internal ID20880512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:11995342..11997754hg38UCSC Ensembl
chr16:12089199..12091611hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg382413
hg192413
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18028660
Samples
Known GenesSNX29
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6507224
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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