A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6503060



Internal ID20876311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10332991..10347252hg38UCSC Ensembl
chr16:10426848..10441109hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3814262
hg1914262
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18028267
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6503060
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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