A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3185529



Internal ID22338721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:182830874..182835527hg38UCSC Ensembl
chr4:183752027..183756680hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg384654
hg194654
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6994n152
Supporting Variantsnssv14434315
SamplesHG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3185529
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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