A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv725027



Internal ID16018983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:158755774..158758153hg38UCSC Ensembl
Innerchr1:158725564..158727943hg19UCSC Ensembl
Innerchr1:156992188..156994567hg18UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg382380
hg192380
hg182380
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv547999
Supporting Variants
Samples
Known GenesOR6K6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv725027
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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