A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007166



Internal ID19096384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:102192076..102393290hg38UCSC Ensembl
Innerchr1:102657632..102858846hg19UCSC Ensembl
Innerchr1:102430220..102631434hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg38201215
hg19201215
hg18201215
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv210n100
Supporting Variantsnssv3699615, nssv3464706
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)nsv1007166
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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