A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062004



Internal ID19151223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:77697821..77732955hg38UCSC Ensembl
Innerchr16:77731718..77766852hg19UCSC Ensembl
Innerchr16:76289219..76324353hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3835135
hg1935135
hg1835135
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559668
Samples
Known GenesNUDT7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1062004
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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