A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6318633



Internal ID20851725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:187451548..187451855hg38UCSC Ensembl
chr1:187420680..187420987hg19UCSC Ensembl
Cytoband1q31.1
Allele length
AssemblyAllele length
hg38308
hg19308
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18054755
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6318633
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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