A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699751



Internal ID15089717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:81806517..81811086hg38UCSC Ensembl
Innerchr16:81840122..81844691hg19UCSC Ensembl
Innerchr16:80397623..80402192hg18UCSC Ensembl
Innerchr16:80397623..80402192hg17UCSC Ensembl
Cytoband16q23.2
Allele length
AssemblyAllele length
hg384570
hg194570
hg184570
hg174570
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523908
Supporting Variants
Samples
Known GenesPLCG2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699751
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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