A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3559676



Internal ID18857957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:77988026..78046521hg38UCSC Ensembl
Innerchr16:78021923..78080418hg19UCSC Ensembl
Innerchr16:76579424..76637919hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3858496
hg1958496
hg1858496
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1056127
Supporting Variants
Samples
Known GenesCLEC3A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3559676
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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