A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436865



Internal ID21094418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:36269664..36270518hg38UCSC Ensembl
chr9:36269661..36270515hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38855
hg19855
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226430
Samples
Known GenesGNE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436865
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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