A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6351634



Internal ID21009187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:241568633..241569348hg38UCSC Ensembl
chr2:242508048..242508763hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38716
hg19716
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18085154
Samples
Known GenesBOK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6351634
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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