A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003539



Internal ID19092757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:174068577..174098147hg38UCSC Ensembl
Innerchr3:173786367..173815937hg19UCSC Ensembl
Innerchr3:175269061..175298631hg18UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg3829571
hg1929571
hg1829571
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3613617
Samples
Known GenesNLGN1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1003539
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