A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496584



Internal ID20869787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:31199618..31224465hg38UCSC Ensembl
chr16:31210939..31235786hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg3824848
hg1924848
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18028938
Samples
Known GenesC16orf98, PYCARD, PYDC1, TRIM72
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496584
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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