A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006501



Internal ID18749032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:2405571..2615751hg38UCSC Ensembl
Innerchr3:2447255..2657435hg19UCSC Ensembl
Innerchr3:2422255..2632435hg18UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38210181
hg19210181
hg18210181
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3590375
Samples
Known GenesCNTN4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1006501
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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