A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3174579



Internal ID22332890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:61807958..61808088hg38UCSC Ensembl
chr4:62673676..62673806hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14451803
SamplesHG00733
Known GenesLPHN3
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3174579
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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