A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6323726



Internal ID20856847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:213954596..213955812hg38UCSC Ensembl
chr1:214127939..214129155hg19UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg381217
hg191217
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18057789
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6323726
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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