A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv682671



Internal ID15072637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:12172197..12184246hg38UCSC Ensembl
Innerchr11:12193744..12205793hg19UCSC Ensembl
Innerchr11:12150320..12162369hg18UCSC Ensembl
Innerchr11:12150320..12162369hg17UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg3812050
hg1912050
hg1812050
hg1712050
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515573
Supporting Variants
Samples
Known GenesMICAL2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv682671
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