A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3739554



Internal ID18691149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:3979832..4143917hg38UCSC Ensembl
Innerchr3:4021516..4185601hg19UCSC Ensembl
Innerchr3:3996516..4160601hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38164086
hg19164086
hg18164086
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1002432
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)nssv3739554
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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