A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045442



Internal ID19134661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18918775..18940429hg38UCSC Ensembl
Innerchr11:18940322..18961976hg19UCSC Ensembl
Innerchr11:18896898..18918552hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3821655
hg1921655
hg1821655
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1064n100
Supporting Variantsnssv3508240
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)nsv1045442
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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