A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6421607



Internal ID21079160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:17771011..17959018hg38UCSC Ensembl
chr8:17628520..17816527hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38188008
hg19188008
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231347
Samples
Known GenesFGL1, MTUS1, PCM1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6421607
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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