A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004769



Internal ID19093986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:174243233..174275209hg38UCSC Ensembl
Innerchr3:173961023..173992999hg19UCSC Ensembl
Innerchr3:175443717..175475693hg18UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg3831977
hg1931977
hg1831977
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3613619
Samples
Known GenesNLGN1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1004769
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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