A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517014



Internal ID15097621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:49905459..49905609hg38UCSC Ensembl
Innerchr15:50197656..50197806hg19UCSC Ensembl
Innerchr15:47984948..47985098hg18UCSC Ensembl
Innerchr15:47984948..47985098hg17UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38151
hg19151
hg18151
hg17151
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv661676, nssv653303, nssv664524, nssv668404, nssv675108, nssv689334, nssv667248, nssv653617
Samples
Known GenesATP8B4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517014
Frequency
Sample Size2026
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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