A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327238



Internal ID20860375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:109206267..109215956hg38UCSC Ensembl
chr1:109748889..109758578hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg389690
hg199690
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18199240
Samples
Known GenesKIAA1324, SARS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327238
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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