A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064630



Internal ID18807161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:82788067..82798309hg38UCSC Ensembl
Innerchr16:82821672..82831914hg19UCSC Ensembl
Innerchr16:81379173..81389415hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3810243
hg1910243
hg1810243
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3559857
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)nsv1064630
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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