A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6354538



Internal ID21012091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:1641780..2309014hg38UCSC Ensembl
chr2:1645552..2312786hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg38667235
hg19667235
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207336
Samples
Known GenesMYT1L, PXDN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6354538
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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