A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022644



Internal ID19111862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:16092468..16166875hg38UCSC Ensembl
Innerchr8:15949977..16024384hg19UCSC Ensembl
Innerchr8:15994348..16068755hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3874408
hg1974408
hg1874408
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7109n100
Supporting Variantsnssv3675949, nssv3675950
Samples
Known GenesMSR1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022644
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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