A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6323261



Internal ID20856378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:164979842..164982812hg38UCSC Ensembl
chr1:164949079..164952049hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg382971
hg192971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052804
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6323261
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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