A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516224



Internal ID15096831
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:113117152..113117514hg38UCSC Ensembl
Innerchr11:112987874..112988236hg19UCSC Ensembl
Innerchr11:112493084..112493446hg18UCSC Ensembl
Innerchr11:112493084..112493446hg17UCSC Ensembl
Cytoband11q23.1
Allele length
AssemblyAllele length
hg38363
hg19363
hg18363
hg17363
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv662805, nssv657979, nssv681966, nssv666919, nssv658868, nssv662460, nssv686239, nssv691533, nssv670225, nssv673470
Samples
Known GenesNCAM1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516224
Frequency
Sample Size2026
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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