A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044697



Internal ID19133916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:96471617..96550811hg38UCSC Ensembl
Innerchr11:96204781..96283976hg19UCSC Ensembl
Innerchr11:95844429..95923624hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3879195
hg1979196
hg1879196
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1255n100
Supporting Variantsnssv3710713
Samples
Known GenesJRKL-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044697
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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