A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6339927



Internal ID20997480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:133160521..133305633hg38UCSC Ensembl
chr2:133918093..134063205hg19UCSC Ensembl
Cytoband2q21.2
Allele length
AssemblyAllele length
hg38145113
hg19145113
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4128n223
Supporting Variantsnssv18077516
Samples
Known GenesMIR7853, NCKAP5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6339927
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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