A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5624152



Internal ID21572457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:102559376..102559376hg38UCSC Ensembl
chrX:101814304..101814304hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17165004
SamplesHG00171
Known GenesNXF4
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5624152
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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