A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv673390



Internal ID15063356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:44258540..44269934hg38UCSC Ensembl
Innerchr11:44280090..44291484hg19UCSC Ensembl
Innerchr11:44236666..44248060hg18UCSC Ensembl
Innerchr11:44236666..44248060hg17UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3811395
hg1911395
hg1811395
hg1711395
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517357
Supporting Variants
Samples
Known GenesALX4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv673390
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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