A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv16n100



Internal ID20151632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9237601..9351410hg38UCSC Ensembl
chr1:9297660..9411469hg19UCSC Ensembl
chr1:9220247..9334056hg18UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg38113810
hg19113810
hg18113810
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1011354, nsv1013944, nsv1014684, nsv1004906, nsv1006294, nsv1009914, nsv1002217, nsv1010537, nsv1009956, nsv999955
Samples
Known GenesH6PD, SPSB1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv16n100
Frequency
Sample Size29084
Observed Gain17
Observed Loss0
Observed Complex0
Frequencyn/a


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