A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027083



Internal ID18769615
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167281723..167371621hg38UCSC Ensembl
Innerchr6:167695211..167785109hg19UCSC Ensembl
Innerchr6:167615201..167705099hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3889899
hg1989899
hg1889899
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6198n100
Supporting Variantsnssv3655436
Samples
Known GenesTTLL2, UNC93A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1027083
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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