A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006125



Internal ID19095343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:65203548..65232993hg38UCSC Ensembl
Innerchr3:65189223..65218668hg19UCSC Ensembl
Innerchr3:65164263..65193708hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3829446
hg1929446
hg1829446
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4762n100
Supporting Variantsnssv3593869
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1006125
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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