A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv852060



Internal ID15799330
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:1608055..1764390hg38UCSC Ensembl
Innerchr16:1658056..1814391hg19UCSC Ensembl
Innerchr16:1598057..1754392hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38156336
hg19156336
hg18156336
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv571168
Supporting Variants
Samples
Known GenesCRAMP1L, HN1L, IFT140, MAPK8IP3, MIR3177
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv852060
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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