A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6333572



Internal ID20866751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:3900758..3916503hg38UCSC Ensembl
chr1:3817322..3833067hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg3815746
hg1915746
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203070
Samples
Known GenesLINC01134
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6333572
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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