A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3531049



Internal ID18829330
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 StatusS
Merged Variantsnsv1035816
Supporting Variants
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)nssv3531049
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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