A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv676956



Internal ID15413608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:11280317..11284984hg38UCSC Ensembl
Innerchr11:11301864..11306531hg19UCSC Ensembl
Innerchr11:11258440..11263107hg18UCSC Ensembl
Innerchr11:11258440..11263107hg17UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg384668
hg194668
hg184668
hg174668
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519371
Supporting Variants
Samples
Known GenesGALNT18
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv676956
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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