A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058004



Internal ID19147223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:66508526..66596459hg38UCSC Ensembl
Innerchr17:64504644..64592577hg19UCSC Ensembl
Innerchr17:61935106..62023039hg18UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3887934
hg1987934
hg1887934
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3275n100
Supporting Variantsnssv3567735
Samples
Known GenesPRKCA
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058004
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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