A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15752574



Internal ID21392837
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 StatusS
Merged Variantsnsv4432599
Supporting Variants
SamplesSMI041
Known GenesH3F3B, MIR4738, UNK
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15752574
Frequency
Sample Size15
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer