A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6346416



Internal ID21003969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:213752842..213807326hg38UCSC Ensembl
chr2:214617566..214672050hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg3854485
hg1954485
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18083660
Samples
Known GenesSPAG16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6346416
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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