A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999523



Internal ID19159060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:25545970..25571444hg38UCSC Ensembl
Innerchr3:25587461..25612935hg19UCSC Ensembl
Innerchr3:25562465..25587939hg18UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg3825475
hg1925475
hg1825475
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4705n100
Supporting Variantsnssv3589510
Samples
Known GenesRARB
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv999523
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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