A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704970



Internal ID15441622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:128934894..128948897hg38UCSC Ensembl
Innerchr11:128804789..128818792hg19UCSC Ensembl
Innerchr11:128309999..128324002hg18UCSC Ensembl
Innerchr11:128309999..128324002hg17UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg3814004
hg1914004
hg1814004
hg1714004
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528381
Supporting Variants
Samples
Known GenesTP53AIP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704970
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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