A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6353825



Internal ID21011378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:229371739..229396322hg38UCSC Ensembl
chr2:230236455..230261038hg19UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg3824584
hg1924584
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18084791
Samples
Known GenesDNER
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6353825
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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