A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3739654



Internal ID19037935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:24851450..24870539hg38UCSC Ensembl
Innerchr3:24892941..24912030hg19UCSC Ensembl
Innerchr3:24867945..24887034hg18UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg3819090
hg1919090
hg1819090
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1011730
Supporting Variants
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)nssv3739654
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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