A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6323585



Internal ID20856704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:212116536..212117397hg38UCSC Ensembl
chr1:212289878..212290739hg19UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg38862
hg19862
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18199946
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6323585
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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