A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6318994



Internal ID20852086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:21994101..21999400hg38UCSC Ensembl
chr1:22320594..22325893hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg385300
hg195300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv118n223
Supporting Variantsnssv18057860
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6318994
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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