A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6352860



Internal ID21010413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:174404701..174410900hg38UCSC Ensembl
chr2:175269429..175275628hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg386200
hg196200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4192n223
Supporting Variantsnssv18207427
Samples
Known GenesSCRN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6352860
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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