A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004921



Internal ID18747452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:151794802..151824090hg38UCSC Ensembl
Innerchr3:151512590..151541878hg19UCSC Ensembl
Innerchr3:152995280..153024568hg18UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3829289
hg1929289
hg1829289
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4921n100
Supporting Variantsnssv3606305
Samples
Known GenesAADAC, MIR548H2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1004921
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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