A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv56n100



Internal ID19010424
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16559628..16643949hg38UCSC Ensembl
chr1:16886123..16970444hg19UCSC Ensembl
chr1:16758710..16843031hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3884322
hg1984322
hg1884322
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1012484, nsv1010184, nsv997666, nsv1000986, nsv1004437
Samples
Known GenesCROCCP2, NBPF1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv56n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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