A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14435902



Internal ID22179013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:137413370..137413485hg38UCSC Ensembl
chr7:137098116..137098231hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38116
hg19116
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3170839
Supporting Variants
SamplesHG00514
Known GenesDGKI
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14435902
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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