A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6351037



Internal ID21008590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:46256927..46260204hg38UCSC Ensembl
chr2:46484066..46487343hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg383278
hg193278
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18089940
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6351037
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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