A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv150n100



Internal ID22786237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:37167223..37221817hg38UCSC Ensembl
chr1:37632824..37687418hg19UCSC Ensembl
chr1:37405411..37460005hg18UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3854595
hg1954595
hg1854595
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1001914, nsv997970, nsv1003408
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)dgv150n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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