A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15205394



Internal ID21344195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:127720831..127720831hg38UCSC Ensembl
chr9:130483110..130483110hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38432
hg19432
Variant TypeCNV insertion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3939457
Supporting Variants
SamplesHG002
Known GenesTTC16
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15205394
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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