A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3710086



Internal ID19008367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:37564230..37595788hg38UCSC Ensembl
Innerchr11:37585780..37617338hg19UCSC Ensembl
Innerchr11:37542356..37573914hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3831559
hg1931559
hg1831559
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1048448
Supporting Variants
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)nssv3710086
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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