A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4917n100



Internal ID22791004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:145907227..145944673hg38UCSC Ensembl
chr3:145625014..145662460hg19UCSC Ensembl
chr3:147107704..147145150hg18UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3837447
hg1937447
hg1837447
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1003059, nsv1001959, nsv1009264, nsv1014187, nsv1001140, nsv1004210, nsv1010260, nsv1012874
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4917n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss22
Observed Complex0
Frequencyn/a


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