A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036170



Internal ID19125389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18931003..18949189hg38UCSC Ensembl
Innerchr11:18952550..18970736hg19UCSC Ensembl
Innerchr11:18909126..18927312hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3818187
hg1918187
hg1818187
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3503408
Samples
Known GenesMRGPRX1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036170
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer