A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3182408



Internal ID22337085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:152786053..152786217hg38UCSC Ensembl
chr4:153707205..153707369hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg38165
hg19165
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14435516
SamplesHG00514
Known GenesARFIP1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3182408
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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