A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060655



Internal ID18803186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:77762551..77934211hg38UCSC Ensembl
Innerchr16:77796448..77968108hg19UCSC Ensembl
Innerchr16:76353949..76525609hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38171661
hg19171661
hg18171661
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559669
Samples
Known GenesVAT1L
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060655
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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