A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998949



Internal ID18811799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:159057017..159676761hg38UCSC Ensembl
Innerchr3:158774806..159394550hg19UCSC Ensembl
Innerchr3:160257500..160877244hg18UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg38619745
hg19619745
hg18619745
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3606402
Samples
Known GenesIQCJ, IQCJ-SCHIP1, MIR3919, SCHIP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv998949
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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