A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3559263



Internal ID18510858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:53210111..53272427hg38UCSC Ensembl
Innerchr16:53244023..53306339hg19UCSC Ensembl
Innerchr16:51801524..51863840hg18UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg3862317
hg1962317
hg1862317
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1055220
Supporting Variants
Samples
Known GenesCHD9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3559263
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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