A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14402977



Internal ID22326438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:71752481..71752481hg38UCSC Ensembl
chr9:74367397..74367397hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg38174
hg19174
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3553052
Supporting Variants
SamplesNA19240
Known GenesTMEM2
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
CommentsSequences at least 70% masked by tandem repeat finder or contained within a tandem repeat
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14402977
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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