A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703995



Internal ID15440647
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:85013751..85183989hg38UCSC Ensembl
Innerchr11:84724795..84895033hg19UCSC Ensembl
Innerchr11:84402443..84572681hg18UCSC Ensembl
Innerchr11:84402443..84572681hg17UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38170239
hg19170239
hg18170239
hg17170239
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527535
Supporting Variants
Samples
Known GenesDLG2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703995
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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