A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3565953



Internal ID22434662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:148389589..148389589hg38UCSC Ensembl
chrX:147471109..147471109hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14354168, nssv14354169
SamplesHG00732, HG00733
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3565953
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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