A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040695



Internal ID19129914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18918775..18940574hg38UCSC Ensembl
Innerchr11:18940322..18962121hg19UCSC Ensembl
Innerchr11:18896898..18918697hg18UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3821800
hg1921800
hg1821800
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1064n100
Supporting Variantsnssv3506077
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)nsv1040695
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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