A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3173847



Internal ID22332515
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:110705434..110705573hg38UCSC Ensembl
chrX:109948662..109948801hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38140
hg19140
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10235n152
Supporting Variantsnssv14429904
SamplesHG00514
Known GenesCHRDL1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3173847
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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