A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513500



Internal ID20886845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:68333201..68344600hg38UCSC Ensembl
chr16:68367104..68378503hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg3811400
hg1911400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18031697
Samples
Known GenesPRMT7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513500
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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