A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17639034



Internal ID21831081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:47338041..47711913hg38UCSC Ensembl
chrX:47197440..47571312hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg38373873
hg19373873
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6103365
Supporting Variants
Samples
Known GenesARAF, CFP, CXXC1P1, ELK1, MIR4769, SNORA11C, SYN1, TIMP1, UXT, UXT-AS1, ZNF157, ZNF41
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17639034
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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