A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032940



Internal ID19122162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39389580..39511377hg38UCSC Ensembl
Innerchr8:39247099..39368896hg19UCSC Ensembl
Innerchr8:39366256..39488053hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38121798
hg19121798
hg18121798
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7174n100
Supporting Variantsnssv3756695, nssv3756691, nssv3756696, nssv3756692, nssv3756687, nssv3756690, nssv3756688, nssv3756693, nssv3756689, nssv3756694
Samples
Known GenesADAM3A, ADAM5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032940
Frequency
Sample Size11257
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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