A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3710711



Internal ID19008992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:96471617..96546628hg38UCSC Ensembl
Innerchr11:96204781..96279793hg19UCSC Ensembl
Innerchr11:95844429..95919441hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3875012
hg1975013
hg1875013
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1042360
Supporting Variants
Samples
Known GenesJRKL-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3710711
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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