A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6321948



Internal ID20855057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:110091506..110095999hg38UCSC Ensembl
chr1:110634128..110638621hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg384494
hg194494
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18050840
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6321948
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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