A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4435760



Internal ID21397762
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:70037085..70040084hg38UCSC Ensembl
chr9:72652001..72655000hg19UCSC Ensembl
Cytoband9q21.12
Allele length
AssemblyAllele length
hg383000
hg193000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15748341, nssv15749975, nssv15745775, nssv15754442, nssv15749146, nssv15751944, nssv15751154
SamplesSMI034, MDQ045, BTQ038, MDQ010, BTQ016, SMI018, MDQ025
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4435760
Frequency
Sample Size15
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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