A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026690



Internal ID18769221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:150097979..150164447hg38UCSC Ensembl
Innerchr6:150419115..150485583hg19UCSC Ensembl
Innerchr6:150460808..150527276hg18UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3866469
hg1966469
hg1866469
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654467
Samples
Known GenesPPP1R14C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026690
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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