A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700145



Internal ID15436797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:93267146..93380404hg38UCSC Ensembl
InnerchrX:92522145..92635403hg19UCSC Ensembl
InnerchrX:92408801..92522059hg18UCSC Ensembl
InnerchrX:92328290..92441548hg17UCSC Ensembl
CytobandXq21.32
Allele length
AssemblyAllele length
hg38113259
hg19113259
hg18113259
hg17113259
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516563
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700145
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