A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437267



Internal ID21094820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:128935351..128951038hg38UCSC Ensembl
chr9:131697630..131713317hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3815688
hg1915688
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18223693
Samples
Known GenesDOLK, NUP188, PHYHD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437267
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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