A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv683708



Internal ID15073674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:27359837..27364221hg38UCSC Ensembl
Innerchr16:27371158..27375542hg19UCSC Ensembl
Innerchr16:27278659..27283043hg18UCSC Ensembl
Innerchr16:27278659..27283043hg17UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg384385
hg194385
hg184385
hg174385
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)nssv683708
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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