A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999900



Internal ID18812750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:96819697..97180863hg38UCSC Ensembl
Innerchr3:96538541..96899707hg19UCSC Ensembl
Innerchr3:98021231..98382397hg18UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg38361167
hg19361167
hg18361167
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3603318
Samples
Known GenesEPHA6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv999900
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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