A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3188822



Internal ID22340452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:97436080..97461380hg38UCSC Ensembl
chr7:97065392..97090692hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3825301
hg1925301
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14464024, nssv14461314
SamplesHG00733
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3188822
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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