A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3954485



Internal ID21374555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:89484727..89484727hg38UCSC Ensembl
chrX:88739726..88739726hg19UCSC Ensembl
CytobandXq21.31
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15205745
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3954485
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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