A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3733452



Internal ID19031733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:39914089..39973377hg38UCSC Ensembl
Innerchr21:41286014..41345304hg19UCSC Ensembl
Innerchr21:40207884..40267174hg18UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg3859289
hg1959291
hg1859291
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1056677
Supporting Variants
Samples
Known GenesPCP4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3733452
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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