A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013242



Internal ID19102460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:158557789..158588105hg38UCSC Ensembl
Innerchr3:158275578..158305894hg19UCSC Ensembl
Innerchr3:159758272..159788588hg18UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg3830317
hg1930317
hg1830317
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4930n100
Supporting Variantsnssv3606393
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)nsv1013242
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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