A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv690116



Internal ID15080082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:152883607..152932224hg38UCSC Ensembl
InnerchrX:152052151..152100768hg19UCSC Ensembl
InnerchrX:151802807..151851424hg18UCSC Ensembl
InnerchrX:151722719..151771336hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3848618
hg1948618
hg1848618
hg1748618
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517284
Supporting Variants
Samples
Known GenesZNF185
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv690116
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