A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327216



Internal ID20860353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:100289122..100289808hg38UCSC Ensembl
chr1:100754678..100755364hg19UCSC Ensembl
Cytoband1p21.2
Allele length
AssemblyAllele length
hg38687
hg19687
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18049574
Samples
Known GenesRTCA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327216
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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