A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6317898



Internal ID20850988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:78737567..78774057hg38UCSC Ensembl
chr1:79203252..79239742hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3836491
hg1936491
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204470
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6317898
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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