A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048236



Internal ID19137455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:1946041..2001669hg38UCSC Ensembl
Innerchr11:1967271..2022899hg19UCSC Ensembl
Innerchr11:1923847..1979475hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3855629
hg1955629
hg1855629
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1015n100
Supporting Variantsnssv3510705
Samples
Known GenesH19, MIR675, MRPL23, MRPL23-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1048236
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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