A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012835



Internal ID19102052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:162978115..163374121hg38UCSC Ensembl
Innerchr3:162695903..163091909hg19UCSC Ensembl
Innerchr3:164178597..164574603hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38396007
hg19396007
hg18396007
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4967n100
Supporting Variantsnssv3614519
Samples
Known GenesCT64
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1012835
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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