A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3649846



Internal ID18948127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:98099939..98204719hg38UCSC Ensembl
Innerchr6:98547815..98652595hg19UCSC Ensembl
Innerchr6:98654536..98759316hg18UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38104781
hg19104781
hg18104781
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1029201
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)nssv3649846
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