A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1151800



Internal ID15533136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:151793297..151828253hg38UCSC Ensembl
Innerchr3:151511085..151546041hg19UCSC Ensembl
Innerchr3:152993775..153028731hg18UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3834957
hg1934957
hg1834957
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv592049
Supporting Variants
SamplesNINDS_113
Known GenesAADAC, MIR548H2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1151800
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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