A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997859



Internal ID19157395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:164034026..164197553hg38UCSC Ensembl
Innerchr3:163751814..163915341hg19UCSC Ensembl
Innerchr3:165234508..165398035hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38163528
hg19163528
hg18163528
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3614533
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)nsv997859
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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