A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004846



Internal ID19094063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:145095234..145161489hg38UCSC Ensembl
Innerchr2:145852801..145919056hg19UCSC Ensembl
Innerchr2:145569271..145635526hg18UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg3866256
hg1966256
hg1866256
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3582823
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)nsv1004846
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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