A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006124



Internal ID18748655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4235682..4310067hg38UCSC Ensembl
Innerchr3:4277366..4351751hg19UCSC Ensembl
Innerchr3:4252366..4326751hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3874386
hg1974386
hg1874386
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3591633
Samples
Known GenesSETMAR
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1006124
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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