A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3558498



Internal ID22427301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:7622684..7622854hg38UCSC Ensembl
chrX:7540725..7540895hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg38171
hg19171
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14351561, nssv14351560, nssv14351562
SamplesHG00512, HG00513, HG00514
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3558498
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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