A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3557151



Internal ID18855432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:12531870..12544051hg38UCSC Ensembl
Innerchr16:12625727..12637908hg19UCSC Ensembl
Innerchr16:12533228..12545409hg18UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg3812182
hg1912182
hg1812182
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1041164
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)nssv3557151
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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