A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6353200



Internal ID21010753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:241016526..241018812hg38UCSC Ensembl
chr2:241955943..241958229hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg382287
hg192287
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18084572
Samples
Known GenesSNED1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6353200
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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