A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3649839



Internal ID18948120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:95500984..95575048hg38UCSC Ensembl
Innerchr6:95948860..96022924hg19UCSC Ensembl
Innerchr6:96055581..96129645hg18UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3874065
hg1974065
hg1874065
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1031951
Supporting Variants
Samples
Known GenesMANEA-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3649839
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