A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6321525



Internal ID20854632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:234098116..234098765hg38UCSC Ensembl
chr1:234233862..234234511hg19UCSC Ensembl
Cytoband1q42.2
Allele length
AssemblyAllele length
hg38650
hg19650
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202384
Samples
Known GenesSLC35F3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6321525
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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