A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv907251



Internal ID6269178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88494976..88570134hg19UCSC Ensembl
Outerchr16:88482758..88584207hg19UCSC Ensembl
Innerchr16:87022477..87097635hg18UCSC Ensembl
Outerchr16:87010259..87111708hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1544311
SamplesMS16315
Known GenesZFPM1, ZNF469
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv907251
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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