A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6139024



Internal ID338208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:118439363..118439862hg38UCSC Ensembl
chrX:117573326..117573825hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17737276
Samples
Known GenesWDR44
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6139024
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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