A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6347763



Internal ID21005316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:105206701..105210200hg38UCSC Ensembl
chr2:105823158..105826657hg19UCSC Ensembl
Cytoband2q12.1
Allele length
AssemblyAllele length
hg383500
hg193500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205810
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6347763
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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