A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3175417



Internal ID22333349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:35576159..35576221hg38UCSC Ensembl
chr1:36041760..36041822hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14395424
SamplesNA19240
Known GenesTFAP2E
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3175417
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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