A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007902



Internal ID19097121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:154571387..154727150hg38UCSC Ensembl
Innerchr3:154289176..154444939hg19UCSC Ensembl
Innerchr3:155771870..155927633hg18UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg38155764
hg19155764
hg18155764
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4925n100
Supporting Variantsnssv3606345, nssv3606346
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)nsv1007902
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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