A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3511756



Internal ID18810037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:88711267..88750552hg38UCSC Ensembl
Innerchr11:88444435..88483720hg19UCSC Ensembl
Innerchr11:88084083..88123368hg18UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg3839286
hg1939286
hg1839286
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1040111
Supporting Variants
Samples
Known GenesGRM5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3511756
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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