A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2761847



Internal ID17453366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:192270898..192280073hg38UCSC Ensembl
Innerchr3:191988687..191997862hg19UCSC Ensembl
Innerchr3:193471381..193480556hg18UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg389176
hg199176
hg189176
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv963555
Supporting Variants
SamplesHGDP00778
Known GenesFGF12
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2761847
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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