A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6338662



Internal ID20996215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:196054207..196061573hg38UCSC Ensembl
chr2:196918931..196926297hg19UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg387367
hg197367
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18081953
Samples
Known GenesDNAH7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6338662
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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