A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6507128



Internal ID20880416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88291375..88293412hg38UCSC Ensembl
chr16:88324981..88327018hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg382038
hg192038
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18033173
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6507128
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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