A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018397



Internal ID19107614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:20893016..20934215hg38UCSC Ensembl
Innerchr6:20893247..20934446hg19UCSC Ensembl
Innerchr6:21001226..21042425hg18UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3841200
hg1941200
hg1841200
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654822
Samples
Known GenesCDKAL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018397
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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