A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004897



Internal ID19094114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:1041816..1200543hg38UCSC Ensembl
Innerchr3:1083500..1242227hg19UCSC Ensembl
Innerchr3:1058500..1217227hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38158728
hg19158728
hg18158728
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3590294
Samples
Known GenesCNTN6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1004897
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer