A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011748



Internal ID19100966
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:66747695..66781251hg38UCSC Ensembl
Innerchr4:67613413..67646969hg19UCSC Ensembl
Innerchr4:67296008..67329564hg18UCSC Ensembl
Cytoband4q13.2
Allele length
AssemblyAllele length
hg3833557
hg1933557
hg1833557
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3626066
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)nsv1011748
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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