A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv659649



Internal ID15396301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:34973043..35012937hg38UCSC Ensembl
InnerchrX:34991160..35031054hg19UCSC Ensembl
InnerchrX:34901081..34940975hg18UCSC Ensembl
InnerchrX:34750817..34790711hg17UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg3839895
hg1939895
hg1839895
hg1739895
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517572
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv659649
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