A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039556



Internal ID19128775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18914707..18939619hg38UCSC Ensembl
Innerchr11:18936254..18961166hg19UCSC Ensembl
Innerchr11:18892830..18917742hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3824913
hg1924913
hg1824913
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1061n100
Supporting Variantsnssv3506042
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)nsv1039556
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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