A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3654288



Internal ID18952569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:110064994..110095665hg38UCSC Ensembl
Innerchr6:110386197..110416868hg19UCSC Ensembl
Innerchr6:110492890..110523561hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3830672
hg1930672
hg1830672
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1023185
Supporting Variants
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)nssv3654288
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