A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6328264



Internal ID20861410
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:219950201..219953300hg38UCSC Ensembl
chr1:220123543..220126642hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg383100
hg193100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18057862
Samples
Known GenesRNU5F-1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6328264
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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