A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv652951



Internal ID15389603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:39221237..39248033hg38UCSC Ensembl
InnerchrX:39080490..39107286hg19UCSC Ensembl
InnerchrX:38965434..38992230hg18UCSC Ensembl
InnerchrX:38836706..38863502hg17UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg3826797
hg1926797
hg1826797
hg1726797
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517716
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv652951
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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