A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572385



Internal ID16013108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:35349255..36051211hg38UCSC Ensembl
Innerchr16:34583626..35285582hg19UCSC Ensembl
Innerchr16:34441127..35143083hg18UCSC Ensembl
Cytoband16p11.1
Allele length
AssemblyAllele length
hg38701957
hg19701957
hg18701957
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv856261
Samples
Known GenesFLJ26245, LOC100130700, LOC146481, LOC283914
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572385
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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