A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045282



Internal ID19134501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:1946041..2043381hg38UCSC Ensembl
Innerchr11:1967271..2064611hg19UCSC Ensembl
Innerchr11:1923847..2021187hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3897341
hg1997341
hg1897341
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1016n100
Supporting Variantsnssv3508349, nssv3522697, nssv3511036, nssv3517636
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)nsv1045282
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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