A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013962



Internal ID19103181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:40037495..40154815hg38UCSC Ensembl
Innerchr3:40078986..40196306hg19UCSC Ensembl
Innerchr3:40053990..40171310hg18UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38117321
hg19117321
hg18117321
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3589694
Samples
Known GenesMYRIP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013962
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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