A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv143n100



Internal ID22786230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:30090604..30706742hg38UCSC Ensembl
chr1:30563451..31179589hg19UCSC Ensembl
chr1:30336038..30952176hg18UCSC Ensembl
Cytoband1p35.2
Allele length
AssemblyAllele length
hg38616139
hg19616139
hg18616139
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1005851, nsv1001237
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)dgv143n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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