A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514649



Internal ID20888004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:31423273..31425099hg38UCSC Ensembl
chr16:31434594..31436420hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381827
hg191827
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18028951
Samples
Known GenesITGAD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514649
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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