A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14439329



Internal ID22232066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:151915916..151917285hg38UCSC Ensembl
chrX:151084388..151085757hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg381370
hg191370
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3180712
Supporting Variants
SamplesHG00733
Known GenesMAGEA4
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14439329
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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