A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6503693



Internal ID20876949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:31424860..31425374hg38UCSC Ensembl
chr16:31436181..31436695hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38515
hg19515
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18028952
Samples
Known GenesITGAD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6503693
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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