A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6315778



Internal ID20848851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:158486368..158502412hg38UCSC Ensembl
chr1:158456158..158472202hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg3816045
hg1916045
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200949
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6315778
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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