A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6345206



Internal ID21002759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:229399439..229400093hg38UCSC Ensembl
chr2:230264155..230264809hg19UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg38655
hg19655
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18084796
Samples
Known GenesDNER
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6345206
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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