A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3657486



Internal ID18609081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:55113730..55135540hg38UCSC Ensembl
Innerchr6:54978528..55000338hg19UCSC Ensembl
Innerchr6:55086487..55108297hg18UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3821811
hg1921811
hg1821811
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1033543
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)nssv3657486
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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