A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3180590



Internal ID22336140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:87794711..87795385hg38UCSC Ensembl
chr4:88715863..88716537hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38675
hg19675
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14451906
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)nsv3180590
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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