A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3548173



Internal ID18846454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:22430641..22692541hg38UCSC Ensembl
Innerchr16:22441962..22703862hg19UCSC Ensembl
Innerchr16:22349463..22611363hg18UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg38261901
hg19261901
hg18261901
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1044056
Supporting Variants
Samples
Known GenesLOC100190986, LOC653786, NPIPB5, RRN3P3, SMG1P1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3548173
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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