A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6343601



Internal ID21001154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:162233501..162238200hg38UCSC Ensembl
chr2:163090011..163094710hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg384700
hg194700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207325
Samples
Known GenesFAP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6343601
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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