A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6318833



Internal ID20851925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:165629172..165630750hg38UCSC Ensembl
chr1:165598409..165599987hg19UCSC Ensembl
Cytoband1q24.1
Allele length
AssemblyAllele length
hg381579
hg191579
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052840
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6318833
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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