A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6349996



Internal ID21007549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:187075291..187428332hg38UCSC Ensembl
chr2:187940018..188293059hg19UCSC Ensembl
Cytoband2q32.1
Allele length
AssemblyAllele length
hg38353042
hg19353042
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18080735
Samples
Known GenesCALCRL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6349996
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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