A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496227



Internal ID20869427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:81105422..81122796hg38UCSC Ensembl
chr16:81139027..81156401hg19UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg3817375
hg1917375
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18032808
Samples
Known GenesPKD1L2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496227
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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