A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6334900



Internal ID20868089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:54505151..54519638hg38UCSC Ensembl
chr1:54970824..54985311hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg3814488
hg1914488
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201474
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6334900
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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