A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5670202



Internal ID21618509
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:17619311..17620042hg38UCSC Ensembl
chrX:17637431..17638162hg19UCSC Ensembl
CytobandXp22.13
Allele length
AssemblyAllele length
hg38732
hg19732
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17166154
SamplesNA19239
Known GenesNHS
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5670202
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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