A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998974



Internal ID18811824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:108720592..108813290hg38UCSC Ensembl
Innerchr3:108439439..108532137hg19UCSC Ensembl
Innerchr3:109922129..110014827hg18UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg3892699
hg1992699
hg1892699
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3604400
Samples
Known GenesRETNLB
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv998974
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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