A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999401



Internal ID19158938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:12960142..12984456hg38UCSC Ensembl
Innerchr3:13001642..13025956hg19UCSC Ensembl
Innerchr3:12976642..13000956hg18UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3824315
hg1924315
hg1824315
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3593081
Samples
Known GenesIQSEC1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv999401
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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