A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6335874



Internal ID20993427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:196577791..196578219hg38UCSC Ensembl
chr2:197442515..197442943hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg38429
hg19429
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18081972
Samples
Known GenesHECW2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6335874
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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