A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999408



Internal ID19158945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:158562296..158598642hg38UCSC Ensembl
Innerchr3:158280085..158316431hg19UCSC Ensembl
Innerchr3:159762779..159799125hg18UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg3836347
hg1936347
hg1836347
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3606396
Samples
Known GenesLOC100996447, MLF1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv999408
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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