A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv675166



Internal ID15065132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88713767..88755993hg38UCSC Ensembl
Innerchr16:88780175..88822401hg19UCSC Ensembl
Innerchr16:87307676..87349902hg18UCSC Ensembl
Innerchr16:87307676..87349902hg17UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3842227
hg1942227
hg1842227
hg1742227
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517643
Supporting Variants
Samples
Known GenesCTU2, LOC100289580, MIR4722, PIEZO1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv675166
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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