A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3950721



Internal ID21370790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:132044702..132044702hg38UCSC Ensembl
chrX:131178730..131178730hg19UCSC Ensembl
CytobandXq26.2
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15206083
SamplesHG002
Known GenesMST4
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3950721
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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