A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6333247



Internal ID20866423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:158485382..158544049hg38UCSC Ensembl
chr1:158455172..158513839hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg3858668
hg1958668
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv396n223
Supporting Variantsnssv18053034
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6333247
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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