A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14465504



Internal ID22217817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:17580781..17580862hg38UCSC Ensembl
chrX:17598902..17598983hg19UCSC Ensembl
CytobandXp22.13
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3190009
Supporting Variants
SamplesHG00733
Known GenesNHS
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14465504
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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