A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17645505



Internal ID21837552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:29581981..29590926hg38UCSC Ensembl
chrX:29600098..29609043hg19UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg388946
hg198946
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6100597
Supporting Variants
Samples
Known GenesIL1RAPL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17645505
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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