A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004227



Internal ID19093444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:99032527..99084948hg38UCSC Ensembl
Innerchr3:98751371..98803792hg19UCSC Ensembl
Innerchr3:100234061..100286482hg18UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg3852422
hg1952422
hg1852422
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3603324
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)nsv1004227
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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