A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6331728



Internal ID20864894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:77807699..77816866hg38UCSC Ensembl
chr1:78273384..78282551hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg389168
hg199168
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204455
Samples
Known GenesFAM73A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6331728
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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