A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523178



Internal ID15450471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:26534116..26539960hg38UCSC Ensembl
Innerchr10:26823045..26828889hg19UCSC Ensembl
Innerchr10:26863051..26868895hg18UCSC Ensembl
Innerchr10:26863051..26868895hg17UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg385845
hg195845
hg185845
hg175845
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698891
Samples
Known GenesAPBB1IP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523178
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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