A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038257



Internal ID19127476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18147863..18176762hg38UCSC Ensembl
Innerchr11:18169410..18198309hg19UCSC Ensembl
Innerchr11:18125986..18154885hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3828900
hg1928900
hg1828900
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3708522
Samples
Known GenesMRGPRX4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1038257
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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