A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6351935



Internal ID21009488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:197734301..197741700hg38UCSC Ensembl
chr2:198599025..198606424hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg387400
hg197400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4249n223
Supporting Variantsnssv18084234
Samples
Known GenesBOLL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6351935
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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