A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv659516



Internal ID15049482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:51809788..51975221hg38UCSC Ensembl
InnerchrX:51552884..51718317hg19UCSC Ensembl
InnerchrX:51569624..51735057hg18UCSC Ensembl
InnerchrX:51385920..51551353hg17UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg38165434
hg19165434
hg18165434
hg17165434
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516643
Supporting Variants
Samples
Known GenesMAGED1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv659516
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