A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3177866



Internal ID22334665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:37940281..37940770hg38UCSC Ensembl
chrX:37799534..37800023hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg38490
hg19490
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14464634
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)nsv3177866
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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