A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3710604



Internal ID19008885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:55918323..55964217hg38UCSC Ensembl
Innerchr11:55685799..55731693hg19UCSC Ensembl
Innerchr11:55442375..55488269hg18UCSC Ensembl
Cytoband11q11
Allele length
AssemblyAllele length
hg3845895
hg1945895
hg1845895
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1037046
Supporting Variants
Samples
Known GenesOR5I1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3710604
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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