A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3559858



Internal ID18511453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:82886085..82902066hg38UCSC Ensembl
Innerchr16:82919690..82935671hg19UCSC Ensembl
Innerchr16:81477191..81493172hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3815982
hg1915982
hg1815982
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1064158
Supporting Variants
Samples
Known GenesCDH13
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3559858
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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