A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6341644



Internal ID20999197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:214233701..214256900hg38UCSC Ensembl
chr2:215098425..215121624hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg3823200
hg1923200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4277n223
Supporting Variantsnssv18208164
Samples
Known GenesSPAG16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6341644
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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