A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523155



Internal ID15450448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:226047182..226052129hg38UCSC Ensembl
Innerchr1:226234883..226239830hg19UCSC Ensembl
Innerchr1:224301506..224306453hg18UCSC Ensembl
Innerchr1:222541618..222546565hg17UCSC Ensembl
Cytoband1q42.12
Allele length
AssemblyAllele length
hg384948
hg194948
hg184948
hg174948
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698864
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523155
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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