A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6502773



Internal ID20876021
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:88731957..88782051hg38UCSC Ensembl
chr16:88798365..88848459hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3850095
hg1950095
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18033224
Samples
Known GenesLOC100289580, PIEZO1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6502773
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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