A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044627



Internal ID19133846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:37324332..37360412hg38UCSC Ensembl
Innerchr11:37345882..37381962hg19UCSC Ensembl
Innerchr11:37302458..37338538hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3836081
hg1936081
hg1836081
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1097n100
Supporting Variantsnssv3522186, nssv3513145
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044627
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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