A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700397



Internal ID15437049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:20085633..20097827hg38UCSC Ensembl
Innerchr11:20107179..20119373hg19UCSC Ensembl
Innerchr11:20063755..20075949hg18UCSC Ensembl
Innerchr11:20063755..20075949hg17UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3812195
hg1912195
hg1812195
hg1712195
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524463
Supporting Variants
Samples
Known GenesNAV2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700397
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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