A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3938007



Internal ID21358076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:45121761..45121761hg38UCSC Ensembl
chrX:44981006..44981006hg19UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg381149
hg191149
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15205689
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3938007
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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