A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6318029



Internal ID20851120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:776801..788600hg38UCSC Ensembl
chr1:712181..723980hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3811800
hg1911800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204450
Samples
Known GenesLOC100288069
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6318029
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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