A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705176



Internal ID15095142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:17329494..17484959hg38UCSC Ensembl
InnerchrX:17347617..17503082hg19UCSC Ensembl
InnerchrX:17257538..17413003hg18UCSC Ensembl
InnerchrX:17107274..17262739hg17UCSC Ensembl
CytobandXp22.13
Allele length
AssemblyAllele length
hg38155466
hg19155466
hg18155466
hg17155466
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528560
Supporting Variants
Samples
Known GenesMIR4768, NHS
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705176
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