A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6341792



Internal ID20999345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:213727868..213740234hg38UCSC Ensembl
chr2:214592592..214604958hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg3812367
hg1912367
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18083658
Samples
Known GenesSPAG16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6341792
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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