A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001277



Internal ID19090494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:178067836..178119433hg38UCSC Ensembl
Innerchr3:177785624..177837221hg19UCSC Ensembl
Innerchr3:179268318..179319915hg18UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3851598
hg1951598
hg1851598
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3614985
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)nsv1001277
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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