A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3506685



Internal ID18804966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:135018448..135074876hg38UCSC Ensembl
Innerchr11:134888342..134944770hg19UCSC Ensembl
Innerchr11:134393552..134449982hg18UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3856429
hg1956429
hg1856431
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1041763
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)nssv3506685
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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