A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3182806



Internal ID22337292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:39776530..39776654hg38UCSC Ensembl
chrX:39635784..39635908hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14372887, nssv14413412
SamplesNA19240, HG00514
Known Genes
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3182806
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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