A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3176677



Internal ID22334005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:125390496..125390616hg38UCSC Ensembl
chrX:124524345..124524465hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg38121
hg19121
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14412663
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)nsv3176677
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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