A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037788



Internal ID19127007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:37057170..37105268hg38UCSC Ensembl
Innerchr11:37078720..37126818hg19UCSC Ensembl
Innerchr11:37035296..37083394hg18UCSC Ensembl
Cytoband11p12
Allele length
AssemblyAllele length
hg3848099
hg1948099
hg1848099
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3710082
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)nsv1037788
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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