A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3521716



Internal ID18819997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:86238768..86305399hg38UCSC Ensembl
Innerchr10:87998525..88065156hg19UCSC Ensembl
Innerchr10:87988505..88055136hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg3866632
hg1966632
hg1866632
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1051761
Supporting Variants
Samples
Known GenesGRID1, MIR346
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3521716
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