A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14388953



Internal ID22300417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:137439701..137452800hg38UCSC Ensembl
chr9:140334153..140347252hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3813100
hg1913100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3230262
Supporting Variants
SamplesNA19240
Known GenesENTPD8, MIR7114, NSMF
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14388953
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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