A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496848



Internal ID20870051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:12375980..12385063hg38UCSC Ensembl
chr16:12469837..12478920hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg389084
hg199084
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18028692
Samples
Known GenesSNX29
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496848
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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