A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018062



Internal ID18760595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:53977790..54060394hg38UCSC Ensembl
Innerchr6:53842588..53925192hg19UCSC Ensembl
Innerchr6:53950547..54033151hg18UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3882605
hg1982605
hg1882605
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3657478
Samples
Known GenesMLIP, MLIP-IT1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018062
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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