A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv107n100



Internal ID20151723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16850538..16977337hg38UCSC Ensembl
chr1:17177033..17303832hg19UCSC Ensembl
chr1:17049620..17176419hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38126800
hg19126800
hg18126800
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1013621, nsv999751, nsv1006648, nsv1005053, nsv1002758
Samples
Known GenesCROCC, MFAP2, MIR3675
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv107n100
Frequency
Sample Size29084
Observed Gain14
Observed Loss0
Observed Complex0
Frequencyn/a


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