A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011105



Internal ID18753639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:84172703..84208593hg38UCSC Ensembl
Innerchr1:84638386..84674276hg19UCSC Ensembl
Innerchr1:84410974..84446864hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3835891
hg1935891
hg1835891
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3471116
Samples
Known GenesPRKACB
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1011105
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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