A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327209



Internal ID20860346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:63164167..63193021hg38UCSC Ensembl
chr1:63629838..63658692hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3828855
hg1928855
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203670
Samples
Known GenesLINC00466
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327209
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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