A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14402631



Internal ID22292340
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:141375934..141376195hg38UCSC Ensembl
chr7:141075734..141075995hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38262
hg19262
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3182882
Supporting Variants
SamplesNA19240
Known GenesTMEM178B
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14402631
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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