A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014809



Internal ID19104026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:20983163..21018844hg38UCSC Ensembl
Innerchr3:21024655..21060336hg19UCSC Ensembl
Innerchr3:20999659..21035340hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3835682
hg1935682
hg1835682
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3593103
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)nsv1014809
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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