A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14429120



Internal ID22170675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:36115351..36115828hg38UCSC Ensembl
chrX:36133468..36133945hg19UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg38478
hg19478
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3170917
Supporting Variants
SamplesHG00514
Known GenesCHDC2
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14429120
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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