A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702281



Internal ID15092247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:152904829..152929034hg38UCSC Ensembl
InnerchrX:152073373..152097578hg19UCSC Ensembl
InnerchrX:151824029..151848234hg18UCSC Ensembl
InnerchrX:151743941..151768146hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3824206
hg1924206
hg1824206
hg1724206
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)nssv702281
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