A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332177



Internal ID20865346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:35170868..35183340hg38UCSC Ensembl
chr1:35636469..35648941hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3812473
hg1912473
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203633
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332177
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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