A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3207752



Internal ID22356094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:37876629..37888537hg38UCSC Ensembl
OuterchrX:37735882..37747790hg19UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg3811909
hg1911909
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14268919
SamplesHG00731
Known Genes
MethodOptical mapping
AnalysisBioNano Genomics proprietary analysis
PlatformBioNano Genomics
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3207752
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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