A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3478565



Internal ID19068165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:4968144..4995791hg38UCSC Ensembl
Innerchr1:5028204..5055851hg19UCSC Ensembl
Innerchr1:4928064..4955711hg18UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg3827648
hg1927648
hg1827648
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1014919
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)nssv3478565
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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