A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4432599



Internal ID21394601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:75773920..75786919hg38UCSC Ensembl
chr17:73770001..73783000hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3813000
hg1913000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15752574
SamplesSMI041
Known GenesH3F3B, MIR4738, UNK
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nsv4432599
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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