A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170421



Internal ID22330739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:2761609..2761686hg38UCSC Ensembl
chr4:2763336..2763413hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3878
hg1978
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14451749, nssv14424825
SamplesHG00733, HG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3170421
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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