A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6316076



Internal ID20849153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:27175098..27181510hg38UCSC Ensembl
chr1:27501589..27508001hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg386413
hg196413
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203494
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6316076
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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