A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020313



Internal ID19109532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:91276024..91420431hg38UCSC Ensembl
Innerchr6:91985742..92130149hg19UCSC Ensembl
Innerchr6:92042463..92186870hg18UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38144408
hg19144408
hg18144408
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6090n100
Supporting Variantsnssv3648960
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)nsv1020313
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