A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3559582



Internal ID18511177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:75489056..75538815hg38UCSC Ensembl
Innerchr16:75522954..75572713hg19UCSC Ensembl
Innerchr16:74080455..74130214hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3849760
hg1949760
hg1849760
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1059777
Supporting Variants
Samples
Known GenesCHST5, CHST6, TMEM231
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3559582
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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