A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037131



Internal ID19126350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:10380451..10408451hg38UCSC Ensembl
Innerchr11:10401998..10429998hg19UCSC Ensembl
Innerchr11:10358574..10386574hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3828001
hg1928001
hg1828001
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3708516
Samples
Known GenesCAND1.11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037131
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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