A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1014255



Internal ID18756789
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:158641071..159050753hg38UCSC Ensembl
Innerchr3:158358860..158768542hg19UCSC Ensembl
Innerchr3:159841554..160251236hg18UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg38409683
hg19409683
hg18409683
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3741555
Samples
Known GenesGFM1, LXN, MFSD1, RARRES1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1014255
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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