A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014919



Internal ID19104136
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 StatusM
Merged Variants
Supporting Variantsnssv3478565
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)nsv1014919
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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