A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447606



Internal ID21105159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:136771001..136807700hg38UCSC Ensembl
chr9:139665453..139702152hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3836700
hg1936700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7961n223
Supporting Variantsnssv18227852
Samples
Known GenesCCDC183, CCDC183-AS1, TMEM141
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447606
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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