A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6345728



Internal ID21003281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:195653101..195659000hg38UCSC Ensembl
chr2:196517825..196523724hg19UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg385900
hg195900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206097
Samples
Known GenesSLC39A10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6345728
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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