A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064559



Internal ID18807090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:22916073..22933079hg38UCSC Ensembl
Innerchr16:22927394..22944400hg19UCSC Ensembl
Innerchr16:22834895..22851901hg18UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3817007
hg1917007
hg1817007
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3549120
Samples
Known GenesHS3ST2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1064559
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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