A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6353805



Internal ID21011358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:109558654..109562627hg38UCSC Ensembl
chr2:110316231..110320204hg19UCSC Ensembl
Cytoband2q13
Allele length
AssemblyAllele length
hg383974
hg193974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18075360
Samples
Known GenesSEPT10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6353805
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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