A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058702



Internal ID19147921
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:78882364..79039524hg38UCSC Ensembl
Innerchr16:78916261..79073421hg19UCSC Ensembl
Innerchr16:77473762..77630922hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg38157161
hg19157161
hg18157161
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3719073
Samples
Known GenesWWOX
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058702
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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