A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3171088



Internal ID22331100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:85314271..85316321hg38UCSC Ensembl
chr7:84943587..84945637hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg382051
hg192051
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14456947
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)nsv3171088
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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