A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6345426



Internal ID21002979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:161222501..161224400hg38UCSC Ensembl
chr2:162079012..162080911hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18080594
Samples
Known GenesTANK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6345426
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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