A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002992



Internal ID19092209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:163952648..164217587hg38UCSC Ensembl
Innerchr3:163670436..163935375hg19UCSC Ensembl
Innerchr3:165153130..165418069hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38264940
hg19264940
hg18264940
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3614532
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)nsv1002992
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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