A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5667534



Internal ID21615839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:86623757..86624076hg38UCSC Ensembl
chrX:85878760..85879079hg19UCSC Ensembl
CytobandXq21.2
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17168508
SamplesHG00512
Known GenesDACH2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5667534
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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