A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5622117



Internal ID21570422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:102282011..102282011hg38UCSC Ensembl
chrX:101536968..101536968hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17165002
SamplesHG03732
Known GenesNXF2, NXF2B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5622117
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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