A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18203671



Internal ID20770711
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:63295848..63300884hg38UCSC Ensembl
chr1:63761519..63766555hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg385037
hg195037
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6324911
Supporting Variants
Samples
Known GenesLINC00466
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18203671
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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