A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6330321



Internal ID20863478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:106659530..106696551hg38UCSC Ensembl
chr1:107202152..107239173hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3837022
hg1937022
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18050766
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6330321
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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