A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057600



Internal ID19146819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:78997347..79023531hg38UCSC Ensembl
Innerchr16:79031244..79057428hg19UCSC Ensembl
Innerchr16:77588745..77614929hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3826185
hg1926185
hg1826185
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3040n100
Supporting Variantsnssv3559766
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)nsv1057600
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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