A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997295



Internal ID19156833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:131137011..131200817hg38UCSC Ensembl
Innerchr3:130855855..130919661hg19UCSC Ensembl
Innerchr3:132338545..132402351hg18UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg3863807
hg1963807
hg1863807
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3741467
Samples
Known GenesNEK11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv997295
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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