A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1005502



Internal ID19094719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:104981146..105004995hg38UCSC Ensembl
Innerchr3:104699990..104723839hg19UCSC Ensembl
Innerchr3:106182680..106206529hg18UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg3823850
hg1923850
hg1823850
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3604385
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)nsv1005502
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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