A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705541



Internal ID15442193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:11361795..11369038hg38UCSC Ensembl
Innerchr11:11383342..11390585hg19UCSC Ensembl
Innerchr11:11339918..11347161hg18UCSC Ensembl
Innerchr11:11339918..11347161hg17UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg387244
hg197244
hg187244
hg177244
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528861
Supporting Variants
Samples
Known GenesGALNT18
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705541
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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