A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704881



Internal ID15094847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:131779552..131798641hg38UCSC Ensembl
Innerchr11:131649446..131668535hg19UCSC Ensembl
Innerchr11:131154656..131173745hg18UCSC Ensembl
Innerchr11:131154656..131173745hg17UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3819090
hg1919090
hg1819090
hg1719090
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517550
Supporting Variants
Samples
Known GenesNTM
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704881
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