A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3176162



Internal ID22333741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:132698175..132698233hg38UCSC Ensembl
chr7:132382934..132382992hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14402583, nssv14428205, nssv14463605
SamplesNA19240, HG00733, HG00514
Known GenesFLJ40288
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3176162
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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