A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997811



Internal ID19157348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:65203548..65237259hg38UCSC Ensembl
Innerchr3:65189223..65222934hg19UCSC Ensembl
Innerchr3:65164263..65197974hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3833712
hg1933712
hg1833712
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4762n100
Supporting Variantsnssv3593870, nssv3593871
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)nsv997811
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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