A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6318289



Internal ID20851381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:158982901..158985300hg38UCSC Ensembl
chr1:158952691..158955090hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg382400
hg192400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053480
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6318289
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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