A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6320646



Internal ID20853746
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:84269939..84275372hg38UCSC Ensembl
chr1:84735622..84741055hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg385434
hg195434
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18065043
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6320646
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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