A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14427117



Internal ID22150056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:847822..847907hg38UCSC Ensembl
chr7:887459..887544hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3172808
Supporting Variants
SamplesHG00514
Known GenesSUN1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14427117
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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