A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv210n100



Internal ID22786297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:102180994..102393290hg38UCSC Ensembl
chr1:102646550..102858846hg19UCSC Ensembl
chr1:102419138..102631434hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg38212297
hg19212297
hg18212297
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1000003, nsv1002440, nsv1014058, nsv1003711, nsv1007166, nsv1001712, nsv997714, nsv1012765, nsv1006160, nsv1013397, nsv998426, nsv998908
Samples
Known GenesMIR548AI
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv210n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss43
Observed Complex0
Frequencyn/a


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