A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv678542



Internal ID15068508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167285281..167285890hg38UCSC Ensembl
Innerchr6:167698769..167699378hg19UCSC Ensembl
Innerchr6:167618759..167619368hg18UCSC Ensembl
Innerchr6:167669180..167669789hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38610
hg19610
hg18610
hg17610
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517210
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv678542
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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