A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15205888



Internal ID21344688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:135847949..135847949hg38UCSC Ensembl
chr9:138739795..138739795hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38239
hg19239
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3944021
Supporting Variants
SamplesHG002
Known GenesCAMSAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15205888
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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