A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696324



Internal ID15432976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:69166020..69180698hg38UCSC Ensembl
InnerchrX:68385863..68400541hg19UCSC Ensembl
InnerchrX:68302588..68317266hg18UCSC Ensembl
InnerchrX:68168884..68183562hg17UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg3814679
hg1914679
hg1814679
hg1714679
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518868
Supporting Variants
Samples
Known GenesLINC00269
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696324
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