A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001318



Internal ID19090535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:161698314..161834469hg38UCSC Ensembl
Innerchr3:161416102..161552257hg19UCSC Ensembl
Innerchr3:162898796..163034951hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38136156
hg19136156
hg18136156
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4931n100
Supporting Variantsnssv3606422, nssv3606424, nssv3606423
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)nsv1001318
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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