A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3204437



Internal ID22353287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:90323367..90325381hg38UCSC Ensembl
chrX:89578366..89580380hg19UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg382015
hg192015
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10201n152
Supporting Variantsnssv14352831, nssv14352832, nssv14352833, nssv14352834, nssv14352830
SamplesHG00512, NA19238, NA19239, HG00731, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3204437
Frequency
Sample Size9
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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