A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3557149



Internal ID18855430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:12531870..12543125hg38UCSC Ensembl
Innerchr16:12625727..12636982hg19UCSC Ensembl
Innerchr16:12533228..12544483hg18UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg3811256
hg1911256
hg1811256
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1045473
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)nssv3557149
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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