A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6342978



Internal ID21000531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:119065607..119066260hg38UCSC Ensembl
chr2:119823183..119823836hg19UCSC Ensembl
Cytoband2q14.2
Allele length
AssemblyAllele length
hg38654
hg19654
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18075869
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6342978
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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