A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327086



Internal ID20860223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:27197192..27205793hg38UCSC Ensembl
chr1:27523683..27532284hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg388602
hg198602
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203496
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327086
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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