A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14349370



Internal ID22137770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133828320..133828455hg38UCSC Ensembl
chr9:136693442..136693577hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg38136
hg19136
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3223662
Supporting Variants
SamplesHG00513
Known GenesVAV2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14349370
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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