A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3226181



Internal ID22369073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:57629715..57719408hg38UCSC Ensembl
OuterchrX:57656148..57745841hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg3827565
hg1927565
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14270782
SamplesNA19240
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3226181
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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