A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3199708



Internal ID22349259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:30644309..30651838hg38UCSC Ensembl
chrX:30662426..30669955hg19UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg387530
hg197530
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14350820
SamplesNA19239
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3199708
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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