A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997478



Internal ID19157014
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:79657382..79748717hg38UCSC Ensembl
Innerchr4:80578536..80669871hg19UCSC Ensembl
Innerchr4:80797560..80888895hg18UCSC Ensembl
Cytoband4q21.21
Allele length
AssemblyAllele length
hg3891336
hg1991336
hg1891336
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5330n100
Supporting Variantsnssv3633890, nssv3633889
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)nsv997478
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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