A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5672267



Internal ID21620572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:50795088..50795153hg38UCSC Ensembl
chrX:50538088..50538153hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17167468
SamplesHG00732
Known GenesSHROOM4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5672267
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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