A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017999



Internal ID19107216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:136675630..136844071hg38UCSC Ensembl
Innerchr8:137687873..137856314hg19UCSC Ensembl
Innerchr8:137757055..137925496hg18UCSC Ensembl
Cytoband8q24.23
Allele length
AssemblyAllele length
hg38168442
hg19168442
hg18168442
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7325n100
Supporting Variantsnssv3690001, nssv3757485, nssv3757484, nssv3690002, nssv3690003, nssv3690000
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017999
Frequency
Sample Size11257
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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