A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6336351



Internal ID20993904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:241673292..241707561hg38UCSC Ensembl
chr2:242612707..242646976hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg3834270
hg1934270
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18084847
Samples
Known GenesATG4B, DTYMK, ING5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6336351
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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