A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5963059



Internal ID22737994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:139536239..139536239hg38UCSC Ensembl
chrX:138618398..138618398hg19UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg3850
hg1950
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17440470
Samples
Known GenesF9
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5963059
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer