A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326353



Internal ID20859488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:182998277..183023168hg38UCSC Ensembl
chr1:182967412..182992303hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg3824892
hg1924892
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201746
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326353
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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