A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3468331



Internal ID19062780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:55813023..55829439hg38UCSC Ensembl
Innerchr1:56278696..56295112hg19UCSC Ensembl
Innerchr1:56051284..56067700hg18UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg3816417
hg1916417
hg1816417
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1002958
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)nssv3468331
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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