A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6323548



Internal ID20856667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:103081355..103105413hg38UCSC Ensembl
chr1:103546911..103570969hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3824059
hg1924059
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200320
Samples
Known GenesCOL11A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6323548
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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