A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057946



Internal ID19147165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:29659789..30566163hg38UCSC Ensembl
Innerchr18:27239754..28146129hg19UCSC Ensembl
Innerchr18:25493752..26400127hg18UCSC Ensembl
Cytoband18q12.1
Allele length
AssemblyAllele length
hg38906375
hg19906376
hg18906376
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3725304
Samples
Known GenesMIR302F
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1057946
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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