A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056561



Internal ID19145780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:78002905..78070733hg38UCSC Ensembl
Innerchr16:78036802..78104630hg19UCSC Ensembl
Innerchr16:76594303..76662131hg18UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3867829
hg1967829
hg1867829
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559679
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)nsv1056561
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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