A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1002267



Internal ID19091484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:7811814..7949337hg38UCSC Ensembl
Innerchr3:7853501..7991024hg19UCSC Ensembl
Innerchr3:7828501..7966024hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg38137524
hg19137524
hg18137524
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4676n100
Supporting Variantsnssv3591840, nssv3591839, nssv3591838
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)nsv1002267
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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