A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6353197



Internal ID21010750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:138142701..138146200hg38UCSC Ensembl
chr2:138900271..138903770hg19UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg383500
hg193500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18077218
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6353197
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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