A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1118166



Internal ID15971352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:102041871..102047620hg38UCSC Ensembl
Innerchr8:103054099..103059848hg19UCSC Ensembl
Innerchr8:103123275..103129024hg18UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg385750
hg195750
hg185750
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv611820
Supporting Variants
Samples
Known GenesNCALD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1118166
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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