A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4984n100



Internal ID22791071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:173493576..173571878hg38UCSC Ensembl
chr3:173211366..173289668hg19UCSC Ensembl
chr3:174694060..174772362hg18UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg3878303
hg1978303
hg1878303
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv999363, nsv1010872, nsv997282
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)dgv4984n100
Frequency
Sample Size11257
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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