A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705592



Internal ID15095558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:33168368..33174762hg38UCSC Ensembl
Innerchr6:33136145..33142539hg19UCSC Ensembl
Innerchr6:33244123..33250517hg18UCSC Ensembl
Innerchr6:33244123..33250517hg17UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg386395
hg196395
hg186395
hg176395
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528907
Supporting Variants
Samples
Known GenesCOL11A2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705592
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