A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3557150



Internal ID18855431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:12531870..12543506hg38UCSC Ensembl
Innerchr16:12625727..12637363hg19UCSC Ensembl
Innerchr16:12533228..12544864hg18UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg3811637
hg1911637
hg1811637
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1044975
Supporting Variants
Samples
Known GenesSNX29
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3557150
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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