A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332730



Internal ID20865904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:106451870..106452354hg38UCSC Ensembl
chr1:106994492..106994976hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg38485
hg19485
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18050739
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332730
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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