A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998092



Internal ID19157629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:58512655..58536647hg38UCSC Ensembl
Innerchr1:58978327..59002319hg19UCSC Ensembl
Innerchr1:58750915..58774907hg18UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg3823993
hg1923993
hg1823993
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3465844
Samples
Known GenesOMA1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv998092
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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