A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16292878



Internal ID20502096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:757635..765619hg38UCSC Ensembl
chr12:866801..874785hg19UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg387985
hg197985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4733177
Supporting Variants
Samples
Known GenesWNK1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16292878
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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