A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6506550



Internal ID20879832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:7862501..7929400hg38UCSC Ensembl
chr16:7912503..7979402hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3866900
hg1966900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18032330
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6506550
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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