A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv976768



Internal ID15924038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:151793297..151836961hg38UCSC Ensembl
Innerchr3:151511085..151554749hg19UCSC Ensembl
Innerchr3:152993775..153037439hg18UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3843665
hg1943665
hg1843665
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv592050
Supporting Variants
Samples
Known GenesAADAC, MIR548H2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv976768
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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