A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv692670



Internal ID15082636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:27329738..27339366hg38UCSC Ensembl
Innerchr16:27341059..27350687hg19UCSC Ensembl
Innerchr16:27248560..27258188hg18UCSC Ensembl
Innerchr16:27248560..27258188hg17UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg389629
hg199629
hg189629
hg179629
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516053
Supporting Variants
Samples
Known GenesIL4R
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv692670
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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