A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv570953



Internal ID16011676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:322597..424180hg38UCSC Ensembl
Innerchr16:372597..474180hg19UCSC Ensembl
Innerchr16:312598..414181hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38101584
hg19101584
hg18101584
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4809n54
Supporting Variantsnssv851306
Samples
Known GenesAXIN1, DECR2, LOC100134368, MRPL28, NME4, TMEM8A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv570953
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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