A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6350257



Internal ID21007810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:213932956..214388368hg38UCSC Ensembl
chr2:214797680..215253092hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg38455413
hg19455413
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18083685
Samples
Known GenesSPAG16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6350257
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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