A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6510849



Internal ID20884172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:68331930..68332367hg38UCSC Ensembl
chr16:68365833..68366270hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38438
hg19438
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18031696
Samples
Known GenesPRMT7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6510849
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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