A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3526667



Internal ID22396049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:55930790..55930846hg38UCSC Ensembl
chrX:55957223..55957279hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14351804, nssv14351805
SamplesNA19238, NA19240
Known Genes
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3526667
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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