A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004787



Internal ID19094004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:186668758..186697733hg38UCSC Ensembl
Innerchr3:186386547..186415522hg19UCSC Ensembl
Innerchr3:187869241..187898216hg18UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg3828976
hg1928976
hg1828976
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5003n100
Supporting Variantsnssv3615009
Samples
Known GenesHRG
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1004787
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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