A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3739548



Internal ID18691143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:3399757..3993339hg38UCSC Ensembl
Innerchr3:3441441..4035023hg19UCSC Ensembl
Innerchr3:3416441..4010023hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38593583
hg19593583
hg18593583
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1000460
Supporting Variants
Samples
Known GenesLRRN1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3739548
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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