A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571020



Internal ID16011743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:681725..761746hg38UCSC Ensembl
Innerchr16:731725..811746hg19UCSC Ensembl
Innerchr16:671726..751747hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3880022
hg1980022
hg1880022
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4825n54
Supporting Variantsnssv1149279
Samples1780862416_A
Known GenesCCDC78, FAM173A, FBXL16, HAGHL, JMJD8, METRN, MSLN, NARFL, STUB1, WDR24
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571020
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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