A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4435607



Internal ID21397609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:110797189..110806598hg38UCSC Ensembl
chr9:113559469..113568878hg19UCSC Ensembl
Cytoband9q31.3
Allele length
AssemblyAllele length
hg389410
hg199410
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15753354
SamplesNB08
Known GenesMUSK
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4435607
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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