A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6318194



Internal ID20851285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:158986485..158988607hg38UCSC Ensembl
chr1:158956275..158958397hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg382123
hg192123
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053481
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6318194
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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