A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv40n100



Internal ID20151656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16470226..16660344hg38UCSC Ensembl
chr1:16796721..16986839hg19UCSC Ensembl
chr1:16669308..16859426hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38190119
hg19190119
hg18190119
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1006224, nsv1008610, nsv1013886, nsv998355, nsv997628
Samples
Known GenesCROCCP2, CROCCP3, MIR3675, MST1P2, NBPF1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv40n100
Frequency
Sample Size29084
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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