A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030637



Internal ID18773168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:6687977..6812428hg38UCSC Ensembl
Innerchr8:6545498..6669949hg19UCSC Ensembl
Innerchr8:6532906..6657359hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38124452
hg19124452
hg18124454
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6876n100
Supporting Variantsnssv3753991
Samples
Known GenesAGPAT5, MIR4659A, MIR4659B, XKR5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1030637
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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