A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4435636



Internal ID21397638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:129424722..129439721hg38UCSC Ensembl
chr9:132187001..132202000hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3815000
hg1915000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv864n172
Supporting Variantsnssv15747129, nssv15747641
SamplesNB10, NB09
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4435636
Frequency
Sample Size15
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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