A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035816



Internal ID19125035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:61471083..61486138hg38UCSC Ensembl
Innerchr14:61937801..61952856hg19UCSC Ensembl
Innerchr14:61007554..61022609hg18UCSC Ensembl
Cytoband14q23.1
Allele length
AssemblyAllele length
hg3815056
hg1915056
hg1815056
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3531049
Samples
Known GenesPRKCH
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035816
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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